PlainRecalls

2012 Recall Year Insight

Federal agencies issued 4,173 product recalls indexed by PlainRecalls in calendar year 2012. That represents about 4.00% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 11.4 recalls per day across the FDA, CPSC, USDA FSIS, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 84 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2012.

On this page of 50 records, severity classification shows 11 critical, 37 moderate, and 2 lower-severity recalls. The page references 34 distinct recalling firms operating in 6 distinct product categories, with 48 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), FDA Food (20), FDA Drug (3), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2012 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Moderate Aug 1, 2012

Kettle Brand Potato Chips, Krinkle Cut Cheddar and Sour Cream; 1) 6/2 oz (caddy) item # 0711770000, UPC 0 8114 11715 1; 2) 24/2 oz item # 0711714000, UPC 0 84114 11715 1; 3) 15/5 oz item # 0711718000, UPC 0 84114 11719 9; 4) 12/8.5 oz item #'s 0711726001 and 0711726500 (different numbers for different geographical locations of distribution), UPC 0 84114 11728 1; 5) 10/13 oz item # 0711716001, UPC 0 84114 11717 5; 6) 12/220 g item # 0711915000, UPC 0 84114 1190 5; 7) 10/397g item # 071172

Kettle Foods, Inc.

FDA Food Moderate Aug 1, 2012

Meiko Foods Co. Inc. Cooked Shrimp Balls, 8 oz. Product labeling reads in part:" TOM VIEN COOKED SHRIMP BALLS***MEIKO FOODS CO. INC South El Monte, CA***". The product is packaged in a plastic box liner with a knot tied at the top in a cardboard box.

Meiko Food Company Inc

FDA Food Moderate Aug 1, 2012

21st Century Foods Soy Tempeh, packaged in 12 lb plastic bags and 8 oz containers

21st Century Foods, Inc.

FDA Food Critical Aug 1, 2012

Chocolate, 1pt., UPC 8 52244 00300 8

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Frozen Oyster, Blocks, Wang Brand, 1 lb, packed in plastic bags, 24 bags/case, Item No.: 01356.

Hanmi Incorporated

FDA Food Moderate Aug 1, 2012

Oyster Half Shell Farm, OYS107, 144ps/cs, Oyster Half Shell small Farm, OYS114, 144ps/cs,

Pacific American Fish Co Inc

FDA Food Moderate Aug 1, 2012

Frozen Oyster, IQF, Surasang Brand, 1) 8 oz, packed in plastic bags, 40 bags/case, Item No.: 03777; 2) 2.5 lb, packed in plastic bags, 10 bags/case, Item No.: 06413.

Hanmi Incorporated

FDA Food Moderate Aug 1, 2012

BRD Oyster (Kaki) IQF Farm, BRD 106, 12/2lbs.

Pacific American Fish Co Inc

FDA Food Moderate Aug 1, 2012

Sonoran Rice, 14 lbs (224 oz). Chonita Foods 847 E. 18th St. Tucson, AZ 85719.

Namias dba Chonita Foods

FDA Food Moderate Aug 1, 2012

New England Clam Chowda, pouch 8 lbs., refrigerated. For Institutional Use Only. Mfd. by Plenus Group, Inc., Lowell, MA 01852 Product Number 1023 UPC #: 7 3051691023 3

Plenus Group Inc.

FDA Food Moderate Aug 1, 2012

Kettle Brand Potato Chips, Cheddar Beer, item #0712374000, UPC 0 84114 12375 6.

Kettle Foods, Inc.

FDA Food Critical Aug 1, 2012

Chocolate Dipped Bars, 2 Chocolate & 2 Vanilla, 2.1 fl oz bars, UPC 8 52244 00308 4

Arctic Zero, Inc.

FDA Food Critical Aug 1, 2012

Peppermint Bon Bon Light Ice Cream under the following three brands: Hornbachers, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 41130-21663, Distributed by Supervalu Inc, Eden Prairie, MN 55344. SunnyBrook, Peppermint Bon Bon Light Ice Cream, Half Gallon (1.89 L), UPC 70422-24919, Distributed by Mason Brothers Co., Wadena, MN 56482. Schroeder, Peppermint Bon Bon Ice cream, 56 oz or 1.75 Qt (1.65 L) 3 , UPC 72340-00193, Schroeder Company, Maplewood, MN 55113

Cass Clay Creamery AMPI Fargo Division

FDA Food Moderate Aug 1, 2012

Frozen Oysters are packaged in 8 oz. 40 oz, and 3 lbs. The item numbers are 06413, 03777, FO/HS-OT8; 136300-20110430. The brand names are Z.Shell Sanggul and Z.Shell HS.

B & F, Inc., dba Hanmi, Inc

FDA Food Critical Aug 1, 2012

Strawberry, 1pt., UPC 8 52244 00305 3

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Eden Quality Product Pasteurized Apple Juice from concentrate vitamin C added in a 46 fluid ounce can. Service Size 8 fl oz. Dist. by S. Bertram Inc., Linden, NJ 07036. Concentrate from China.

S Bertram Inc.

FDA Food Critical Aug 1, 2012

Cookies and Cream, 1pt., UPC 8 52244 00303 9

Arctic Zero, Inc.

FDA Food Critical Aug 1, 2012

Arctic Zero, Inc.

FDA Food Critical Aug 1, 2012

Chocolate Dipped Bars 2 Strawberry and 2 Orange Cream, 2.1 Fl oz bars, UPC 8 52244 00309 1

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Oyster Meat Med IQF Farm, OYS101, 10/4lbs., Oyster Meat Large IQF Farm, OYS102, 10/4lbs., Oyster Meat Tiny 8oz IQF Farm, OYS105, 40/8oz.,

Pacific American Fish Co Inc

FDA Drug Low Aug 1, 2012

Tizanidine (Generic for: Zanaflex), 4 mg, 90 Tablets per Bottle, Rx only, , Mfg By: Dr Reddys Labs Ltd., Bachepally, IN 500 - 090, Packaged and distributed by STAT Rx USA, Gainesville, GA, NDC 16590-221-90.

Stat Rx USA

FDA Drug Low Aug 1, 2012

Erythromycin Topical Solution USP, 2%, 60 mL bottle with applicator, Rx only. E. FOUGERA & CO., A division of Fougera Pharmaceuticals, Inc., Melville, New York 11747, NDC 0168-0215-60, UPC 3 0168-0215-60 0.

Fougera Pharmaceuticals, Inc.

FDA Drug Moderate Aug 1, 2012

Dent's Extra Strength Toothache Gum, (benzocaine 20%), Net Wt. .035 Oz.. (1 g) box, C.S. Dent & Co., Erlanger, KY

Grandpa Brands Co

FDA Devices Critical Aug 1, 2012

Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only.

CareFusion 303, Inc.

FDA Devices Moderate Aug 1, 2012

Siemens syngo.plaza. Radiological image processing system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 1, 2012

BridgePoint Medical, Stingray Catheter, REF M - 1000, Sterilized with Ethylene Oxide Gas, Prescription Only, Manufacturer BridgePoint Medical Inc. 13355 10th Ave N, Suite 110, Plymouth, MN 55441. Stingray" Catheters are intended to facilitate the intraluminal placement of conventional guidewires beyond stenotic coronary lesions (including chronic total occlusions) prior to PTCA or stent intervention. When used as part of the BridgePoint Medical System, the Stingray Catheter is intended to fa

Bridgepoint Medical

FDA Devices Moderate Aug 1, 2012

PrepStain Slide Processor. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are intended for use in the screening and detection of cervical cancer, pre-cancerous lesions, atypical cells and all other cytologic categories as defined by The Bethesda System for Reporting Cervical/Vaginal Cytology Diagnoses. The 1.2 DiTi is the tip on the PrepStain to which a pipette tip attaches and dispenses patient samples onto a gla

Tripath Imaging, Inc.

FDA Devices Moderate Aug 1, 2012

VITROS 5600 Integrated System Software For use in the in-vitro quantitative, semi quantitative, and qualitative measurement of variety of analytes of clinical interest.

Ortho-Clinical Diagnostics

FDA Devices Moderate Aug 1, 2012

VITROS 4600 Chemistry System Software For use in the in-vitro quantitative, semi quantitative, and qualitative measurement of variety of analytes of clinical interest.

Ortho-Clinical Diagnostics

FDA Devices Moderate Aug 1, 2012

Product is labeled in part: "***OPTETRAK RBK***TIBIAL TRAY***FINNED, CEMENTED***CoCr Alloy***SIZE 2F/1T***REF 260-04-21***Exactech Gainesville, FL 32653-1630***. The Exactech Optetrak RBK Total Knee System is indicated for use in skeletally mature individuals undergoing primary surgery for knee pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders and/or avascular necrosis of the femoral condyle, post-traumatic loss of the jo

Exactech, Inc.

FDA Devices Moderate Aug 1, 2012

Getinge brand --- large capacity, floor loading jet spray, washers for mechanical washing, intermediate level, thermal disinfection and drying of moisture and temperature stable Hospital case carts, sterilization containers, material handling carts, stands and utensils. --- Model numbers Getinge 9120, 9122, 9125, and 9128

Getinge USA Inc

FDA Devices Moderate Aug 1, 2012

4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S Manufactured or Distributed by Synthes (USA) 1101 Synthes Avenue, Monument CO 80132 4.5MM TI Multiloc Screw Length 38MM-Sterile Ref 04.019,038S. The Multiloc Screw 4.5 is used with a Multiloc PHN for treatment of proximal humerus fractures and is intended to be inserted through the Multiloc PHN until it engages the subchondral bone below the relative distal cortex (cortex closest to the humeral head,

Synthes USA HQ, Inc.

FDA Devices Moderate Aug 1, 2012

Product is labeled in part: "***OPTETRAK***TIBIAL TRAY***TRAPEZOID CEMENTED***Ti Alloy*** SIZE 1F/1T, 2F/1T***FOR CEMENTED USE ONLY***Exactech, Gainesville, FL 32653-1630.***REF 204-04-21***". The Optetrak Comprehensive Knee Systems are indicated for use in skeletally mature individuals undergoing primary surgery for total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis and/or post-traumatic degenerative problems. They are also indicated for revision of failed pre

Exactech, Inc.

FDA Devices Moderate Aug 1, 2012

The Handi-Fil Disposable Syringe Fill Tube is a sterile plastic tube, approximately 10 inches in length, with a "J" shaped curve that projects upward approximately two inches. The Handi-Fil Disposable Syringe Fill Tube is used to transfer radiographic contrast media from a sterile vial to an injection syringe.

Mallinckrodt Inc

FDA Devices Moderate Aug 1, 2012

4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 REF 04.019.028S Manufactured or Distributed by Synthes (USA) 1101 Synthes Avenue, Monument CO 80132 4.5MM TI Multiloc Screw Length 28MM-Sterile Ref 04.019,038S. The Multiloc Screw 4.5 is used with a Multiloc PHN for treatment of proximal humerus fractures and is intended to be inserted through the Multiloc PHN until it engages the subchondral bone below the relative distal cortex (cortex closest to the humeral head,

Synthes USA HQ, Inc.

FDA Devices Moderate Aug 1, 2012

Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery ) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market. They are not intended for use as general hospital beds.

Hill-Rom, Inc.

FDA Devices Critical Aug 1, 2012

Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The devices are intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation. They are n

Respironics, Inc.

FDA Devices Moderate Aug 1, 2012

Leica M525 F50 Surgical Microscope; Article No. 10338422; Leica Microsystems (Schweiz) Ag, 201 Max Schmidheiny Strasse, Heerbrugg, Switzerland Product Usage: The intended use of this device is for improving visibility of objects through magnification and illumination. It can be applied for observation and documentation and for human and veterinary medical treatment.

Leica Microsystems, Inc.

FDA Devices Moderate Aug 1, 2012

Bella Blanket Protective Coverlet, for Mammography, 18cm x 25cm or 24cm x 30cm, Product Code: 311. The purpose of the product is to remove the cold by placing this sheet between the patients breast and the imaging receptor plate.

Beekley Corporation

FDA Devices Moderate Aug 1, 2012

VITROS 5,1 FS System Software For use in the in-vitro quantitative, semi quantitative, and qualitative measurement of variety of analytes of clinical interest.

Ortho-Clinical Diagnostics

FDA Devices Critical Aug 1, 2012

OEC 8800 Flexview, 892.1650 Image-intensified fluoroscopic x-ray system Product Usage: The 8800 Flexview is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical applications may include cholangiography, urologic, endoscopic, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedures. The system may be used for other imaging applications at the physicians discretion.

GE OEC Medical Systems, Inc

FDA Devices Critical Aug 1, 2012

OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures and is also intended for cholangiography, endoscopic, urologic orthopedic, neurologic, vascu

GE OEC Medical Systems, Inc

FDA Devices Moderate Aug 1, 2012

ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp. Mahwah, NJ 07430 Stryker Ireland Carrigtwohill Industrial Estate, Carrigtwohill County Cork, Ireland. The ABG II Modular range of implants is constituted of 8 right stems and 8 left stems. The necks are made of GADS Vitallium, a proprietary Co Cr alloy that Stryker has developed. GADS stands for Gas Atomized Dispersion Strengthened. IT is a Co Cr alloy that is a corrosion resistant and demonstrates qualities of improved fatigue stren

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Aug 1, 2012

NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray system, and has a Part number 989605858501. The device is labeled in part: "***Neusoft***NeuViz16 MULTI-SLICE CT SCANNER SYSTEM***MANUFACTURED FOR NEUSOFT MEDICAL SYSTEMS CO., LTD***MANUFACTURED BY PHILIPS AND NEUSOFT MEDICAL SYSTEMS CO., LTD***ADDRESS: NEUSOFT PARK, HUNNAN INDUSTRIAL AREA, SHENYANG***CHINA***".

Philips And Neusoft Medical Systems Co., Ltd.

FDA Devices Moderate Aug 1, 2012

.***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 1, 2012

PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are intended for use in the screening and detection of cervical cancer, pre-cancerous lesions, atypical cells and all other cytologic categories as defined by The Bethesda System for Reporting Cervical/Vaginal Cytology Diagnoses. The 1.2 DiTi is the tip on the PrepStain to which a pipette tip attaches and dispenses patient samples onto a

Tripath Imaging, Inc.

FDA Devices Moderate Aug 1, 2012

OrthoPediatrics PediLoc Locking Plate System, 4.5mm Contour Locking Compression Femur 8 Hole Plate Right. Used for pediatric patients as indicated for pelvic, small and long bone fractures.

OrthoPediatrics Corp

FDA Devices Moderate Aug 1, 2012

IMPAX CV Reporting The Results Management (RM)/IMPAX CV reporting component facilitates the quick, effective creating of digital structured reports for : adult catheterization and echocardiography, pediatric echocardiography, congenital heat disease, nuclear cardiology and non-invasive vascular disease management. This webb-based application allows cardiology departments to view, edit and sign the structured reports.

AGFA Corp.

FDA Devices Moderate Aug 1, 2012

Hospira LifeShield Latex-Free 100 mL Burette Set, Convertible Pin, 77 inch with 2 Prepierced Injection Sites and Option-Lok Microdrip Soluset with Calibrated Burette and Precision Drip Chamber; an Rx sterile medical device used to administer fluids; 20 individually wrapped sets per case; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 USA; list 12722-65. Intended use: for the administration of fluids.

Hospira Inc.

FDA Devices Moderate Aug 1, 2012

Tibial Punch Tower Assembly. Non-Sterile. CAT NO. 8000-1089. Howmedica Osteonics Corp., 59 Route 17, Allendale, NJ 07401. During primary Scorpio TKA procedures, the Scorpio Tibial Punch Tower (8000-1089) is used in conjunction with Scorpio Tibial Keel Punches (3760-0305/-0709/-1113 and 3761-0305/-0709/-1113) and Tibial Templates (3750-0003/-0005/-0007/-0009/-0013) to prepare the tibia for baseplate implantation. Per the surgical protocol for Duracon and Scorpio Total Knee Systems with X

Stryker Howmedica Osteonics Corp.

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2012 with 2011 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2012

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2012 across the FDA, CPSC, USDA FSIS and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of September 2026.