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 10 critical, 39 moderate, and 1 lower-severity recalls. The page references 32 distinct recalling firms operating in 7 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), FDA Food (17), NHTSA (5), 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 Devices Moderate Aug 8, 2012

Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully automated, high throughput batch analyzer for time- resolved and prompt fluorescence analysis of samples in microtitration plates. It is intended for in vitro quantitative / qualitative determination of analytes in body fluids. The reagent kits running on the GSP instrument are used to test blood specimens dried on filter paper as an aid in screening newborns for congenital di

Perkinelmer

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Pro White Sonic Crest Powered Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

Nextgen Complete Knee Solution Femoral and Provisional Impactor/ Extractor, REF 00-5901-026-00, Non-Sterile Zimmer, Warsaw Indiana The instrument is attached to the femoral implant or provisional to aid in positioning and inserting the components.

Zimmer Inc.

FDA Devices Moderate Aug 8, 2012

Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.

Exactech, Inc.

FDA Devices Moderate Aug 8, 2012

Nextgen Complete Knee Solution Replacement Jaw for Use with Femoral and Provisional Impactor/Extractor, REF 00-5901-026-40, Non-Sterile Zimmer, Warsaw Indiana The instrument is attached to the femoral implant or provisional to aid in positioning and inserting the components.

Zimmer Inc.

FDA Devices Moderate Aug 8, 2012

UroView 2800; MDL number A349855. Product Usage: Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical application may include but are not limited to urologic and endoscopic procedures. The system may be ued for other imaging applications at the physician's discretion.

GE OEC Medical Systems, Inc

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro Clean Re-Charge Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD 9 degree Trial Implant (SJ780T-US) Product Usage: The Aesculap Implant Systems SIBD Trial Implant instruments assist the surgeon in selecting the correct size implant for the patient

Aesculap Implant Systems LLC

FDA Devices Moderate Aug 8, 2012

Cardiac Catheterization Waste Management System w/1000mL Waste Bag, 2 Fluid Admin Sets Product Usage: For waste managment.

ICU Medical, Inc.

FDA Devices Moderate Aug 8, 2012

RF Cannula, 100 mm,Curved 5 MM, 20 G, REF 0406-630-115 RX only, Disposable ( 10/pk) Product Usage: The Stryker RF Cannulae, in combination with the Stryker RF Generator/Multi- Gen and electrodes, are intended for coagulation of soft tissue in orthopedic, arthroscopic, spinal, and neurosurgical applications.

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Pro White Sonic Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

High Pressure Stopcock (3-Way, Luer Lock, Off). Product Usage: For IV.

ICU Medical, Inc.

FDA Devices Moderate Aug 8, 2012

KIT,DISPOSABLE ACCESSORY,3ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.

Intuitive Surgical, Inc.

FDA Devices Moderate Aug 8, 2012

INSTRUMENT ARM DRAPE IS2000, 20 PACK: Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.

Intuitive Surgical, Inc.

FDA Devices Moderate Aug 8, 2012

Beekley O-Spots Floral Skin Markers -Order Number: 752 Product Usage: Mammography Skin Markers for marking: moles, scars, palpable masses or areas of concern

Beekley Corporation

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

The Reliance 130 and 130L Cart Washer/Disinfector is a high capacity mechanical washer intended for use in the washing, low-level disinfecting, and drying of carts, utensils, beds and other miscellaneous reusable items used in the care of patients at healthcare facilities / Crated for shipping.

Steris Corporation

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Pro Clean Sonic Tray BJS Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Pro Clean Sonic Recharge Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

STERRAD Cyclesure Biological Indicator (BI), P/N 14324 are sold in cases, packaged as part of STERRAD System Validation kits and STERRAD test packs. The STERRAD CYCLESURE 24 Biological Indicator (BI), P/N 14324 is intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles.

Advanced Sterilization Products

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro-Clean, various models. Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Moderate Aug 8, 2012

Extraneal and/or DIANEAL LOW CALCIUM Peritoneal Dialysis Solution in Plastic Container, PL-146 used with Automated Peritoneal Dialysis System/Automated PD Set with Cassette; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A. The HomeChoice dialysis system is a personal cycler automated peritoneal dialysis system for pediatric and adult renal patients with fill volumes ranging from 60 mL to 3000 mL. DIANEAL Low Calcium peritoneal dialysis solutions are indicated for us

Baxter Healthcare Renal Div

FDA Devices Moderate Aug 8, 2012

Arm and Hammer Spinbrush ProClean Sonic Recharge Color Wear Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.

Church & Dwight Inc

FDA Devices Critical Aug 8, 2012

Smiths Medical, Medfusion¿ Syringe Infusion Pump, Model 4000, Software Version V1.0 & V1.1, Reorder Numbers 4000-0100-50, 4000-0100-95, 4000-0101-50, 4000-0101-51, and 4000-0101-78. Designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates.

Smiths Medical ASD, Inc.

FDA Devices Moderate Aug 8, 2012

OEC 9800 Plus Digital; MDL number A349855. Product Usage: Is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical applications may include cholangiography, endoscopic, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedures. The system may be used for other imaging applications at the physician's discretion.

GE OEC Medical Systems, Inc

NHTSA No agency class Aug 8, 2012

DODGE 2013: AIR BAGS

DODGE

NHTSA No agency class Aug 8, 2012

CHEVROLET,GMC 2003-2004: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY:FILLER PIPE AND CAP

CHEVROLET,GMC

CPSC No agency class Aug 7, 2012

Children's Pajamas Recalled by My Clothes Due to Violation of Federal Flammability Standard

NHTSA No agency class Aug 3, 2012

CHEVROLET 2008-2012: SUSPENSION:FRONT:CONTROL ARM:LOWER ARM

CHEVROLET

CPSC No agency class Aug 2, 2012

Patio Bistro Sets Sold at Lowe's Stores Recalled Due to Fall Hazard; Made by Midas Lin Co.

Midas Lin Company Ltd., of China

CPSC No agency class Aug 2, 2012

Sears Recalls Kenmore® Dehumidifiers Due to Fire and Burn Hazards

LG Electronics (Tianjin) Appliance Co., Ltd., of Tianjin, China

NHTSA No agency class Aug 2, 2012

FORD 2011-2012: VISIBILITY:WINDSHIELD WIPER/WASHER

FORD

NHTSA No agency class Aug 2, 2012

LEXUS,TOYOTA 2006-2011: SUSPENSION:REAR

LEXUS,TOYOTA

FDA Food Moderate Aug 1, 2012

Korean Molluscan Shellfish (Seasoned Oysters) 250kg, 1000kg

Hamchorom Inc.

FDA Food Moderate Aug 1, 2012

Frozen Yellow Fin Tuna Loins (AAA)Co Treated Skinless Frozen. 44 lbs./carton (3-4 Loins/Case) Imported from Vietnam

East Bay Seafood Co., Inc.

FDA Food Critical Aug 1, 2012

Chocolate Peanut Butter, 1pt., UPC 8 52244 00301 5

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Kettle Brand Potato Chips, Sour Cream and Onion, 12/8.5oz, item # 0711387001, UPC 0 84114 11393 1

Kettle Foods, Inc.

FDA Food Moderate Aug 1, 2012

Nature's Grain Garlic French Bread, 10 oz (284 g) packages,

Southern Bakeries, LLC

FDA Food Critical Aug 1, 2012

Pumpkin Spice, 1pt., UPC 8 52244 00307 7

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Meiko Foods Co. Inc. Cooked Cuttlefish Ball, 2-10 lb bags . Product labeling reads in part:" MEIKO***Muc Vien [Vietnamese] ***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

Meiko Foods Co. Inc. Tempura, 12 oz. Product labeling reads in part:" MEIKO***TEMPURA ***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 Critical Aug 1, 2012

Vanilla Maple, 1pt., UPC 8 52244 00306 0

Arctic Zero, Inc.

FDA Food Moderate Aug 1, 2012

Hidden Valley Salad Crispins Original Ranch; crisp mini-croutons, crunchy carrot bits and a blend of buttermilk and spices; Net Wt. 2.5 Oz. canister, 12 canisters per case; UPC 10071100 008347

Clorox Co (The)

FDA Food Moderate Aug 1, 2012

Meiko Foods Co. Inc. Pollock Fish Balls , 2-10 lb bags. Product labeling reads in part:" MEIKO***POLLOCK FISH BALL S***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

Pediatric electrolyte, Fruit Punch flavor---oral electrolyte solution---helps replace fluids & electrolytes---8 FL OZ (236 mL)---UPC Code: 31191129235 Distributed by Duane Reade/(866)375-6925---440 Ninth Ave., NY, NY 10001---Item #51070-8-4-

Duane Reade Inc

FDA Food Low Aug 1, 2012

"California Girl" Whole Boiled Oysters, 24/8 oz cans.

Atlapac Trading Company Inc

FDA Food Moderate Aug 1, 2012

Kettle Brand Potato Chips, New York Cheddar; 1) 24/1.5oz, item # 0712278000, UPC 0 8114 11271 2; 2) 24/2 oz item # 0703320000 UPC 0 84114 03320 8; 3) 15/5 oz item # 0710863000, UPC 0 84114 0094 1; 4) 12/8.5 oz item #'s 0710813001 and 0710813500 (different numbers for different geographical locations of distribution), UPC 0 84114 10813 5; 5) Canadian item 12/220 g item # 0711920000, UPC 0 84114 11907 0; 6) 100/5 oz as part of a display, item # 0703450000; 7) Shipper containing 48/8.5 oz,

Kettle Foods, Inc.

FDA Food Moderate Aug 1, 2012

New England Clam Chowda Base, pouch 4 lbs., refrigerated. For Institutional Use Only. Mfd. by Plenus Group, Inc., Lowell, MA 01852 Product Number 1010 UPC #: 7 3051691010 3

Plenus Group Inc.

FDA Food Critical Aug 1, 2012

Wellements Baby Move Prune Concentrate with Prebiotics, 4oz., 12 units per case, SKU# 141161, UPC 729609019878.

Wellements, LLC

FDA Food Critical Aug 1, 2012

Coffee, 1pt., UPC 8 52244 00302 2

Arctic Zero, Inc.

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.