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 28 critical, 21 moderate, and 1 lower-severity recalls. The page references 20 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (28), FDA Devices (22), 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 Critical Sep 19, 2012

Mustard Potato Salads: 1) Copperwood Premium Mustard Potato Salad, 2 lbs., 8 11839 01001 2, 5 lbs.; 2) Dairy Fresh Mustard Potato Salad, 0 070163 89090 9, 5 lbs.; 3) Garden Fresh Mustard Potato Salad, l lb., 0 11596 14010 0, 2 lb. 0 11596 24215 6; 4) Market Pantry Mustard Potato Salad, 16 oz., 0 85239 24104 2, 3 lb., 0 85239 24100 4; 5) Spartan Mustard Potato Salad, 1 lb., 0 11213 90319 4, 3 lb., 0 11213 90324; 6) Spoon River Mustard Potato Salad, 3 lb., 0 11596 24207 8; 7) Rogges Mustard Americ

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Italian Pasta Salad: 1) Garden-Fresh Italian Pasta Salad, 8 lbs., 0 11596 92012 4; 2) Market Pantry Italian Pasta Salad 14 oz., 0 85239 20119 0

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Rogges White Potato Salad, 5 lb., 0 11596 51052 1

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Amish Country Cole Slaw, 5 lbs., 0 11596 53010 9;

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Russian Coleslaw is sold at the chef's case, self serve counter, or packaged. Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***RUSSIAN COLESLAW***CABBAGE, CARROTS, THOUSAND DRESSING ( CANOLA MAYONNAISE ( CANOLA OIL, EGGS, FILTERED WATER, HONEY, VINEGAR, SEA SALT, DRY MUSTARD, LEMON JUICE), SWEET PICKLE RELISH ( CUCUMBERS, CRYSTALLIZED CANE JUICE, WATER, DISTILLED VINEGAR, SALT, DEHYDRATED PEPPERS, CALCIUM CHLORIDE, XANTHAN GUM, NATURAL SPICE FLAVORS, GUM ARABIC), SWEET

Ron Stockman Whole Foods

FDA Food Critical Sep 19, 2012

Egg Salad Spreads: 1) Garden-Fresh Egg Salad Spread, 5 lbs., 0 11596 52053 7; 2) Finest Traditions Egg Salad Spread, 12 oz., 7 33147 10491 0 & 4 lbs., 10 733147 10189

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

American Potato Salads: 1) Garden-Fresh American Potato Salad, 1 lb., 0 11596 14015 5, 2 lb., 0 11596 24200 2; 2) Market Pantry American Potato Salad, l lb., 0 85293 24107 3, 3 lb., 0 85239 24102 8; 3) Spartan American Potato Salad, 3 lb., 0 11213 90325 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Family Style Creamy Tuna Salad 5 lbs. 0 11596 55108 1

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Egg Salads: Garden-Fresh Egg Salad, 5 lbs., 0 11596 52022 3 & 5 lbs., 0 11596 52053 Weis Egg Salad, 8 oz., 0 41497 05365 0 & 5 lbs., 0 11596 55221 7

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Black Bean Couscous, 5 lbs., 0 11596 55620 8

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Potato Pancakes 4 lbs. 0 11596 40425 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Acme Classic Potato Salad 16 oz. 0 11596 14030 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Wawa Chicken salad Snack Net Wt. 6.7 oz Distributed by: Wawa, Inc. Wawa, PA 19063 wawa.com On or before August 12; UPC 261902760

Missa Bay, LLC

FDA Food Critical Sep 19, 2012

Gills Onions were used in this product. The product listed below is prepared at Whole Foods Market and distributed in their retail chef's case or on the self-service bar. It was not sold labeled. THREE BEAN SALAD

Ron Stockman Whole Foods

FDA Food Critical Sep 19, 2012

Garden-Fresh Country Style Potato Salad, 5 lb., 0 11596 51075 0

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Black Bean Salsa, 15 oz., 0 11596 06118 4 Garden-Fresh Black Bean Salsa, 5 lbs., 0 11596 52587 7

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Finest Traditions Wild Rice Salad Base, 8 lbs., 10 733147 10183 7

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Gills Onions were used in this product. The product listed below is prepared at Whole Foods Market and distributed in their retail chef's case or on the self-service bar. It was not sold labeled. TEMPEH SALAD

Ron Stockman Whole Foods

FDA Food Critical Sep 19, 2012

Rogges Sour Cream Cuke Salad, 5 lbs., UPC 0 11596 52057 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Gills Onions were used in this product. The product listed below is prepared at Whole Foods Market and distributed in their retail chef's case or on the self-service bar. It was not sold labeled. BEET & GOAT CHEESE SALAD WITH RASPBERRY VINAIGRETTE

Ron Stockman Whole Foods

FDA Food Critical Sep 19, 2012

Finest Traditions Macaroni Salad, 16 oz., 7 33147 00018 2, 3 lbs., 7 33147 00032 8 & 8 lbs., 10 733147 10140 4;

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Homestyle Potato Salads: 1) Acme Homestyle Potato Salad, 2 lbs. 0 11596 34209 2 ; 2) Finest Traditions Homestyle Potato Salad, 16 oz., 7 33147 00019 9, 3 lb., 7 33147 00031 1 , 8 lb., 10 733147 10134 3

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Garden-Fresh Large Diced American Potato Salad, 5 lb., 0 11596 91018 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

The Thousand Island Chicken Salad Roll is sold at the chef's case, self serve counter, or packaged. Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***1000 ISLAND CHICKEN SALAD ROLL 2 FOR 5***BREAD ( UNBLEACHED UNBROMATED WHEAT OR WHOLE WHEAT FLOUR, WATER, FLORIDA CRYSTALS SUGAR, PALM OIL, EGGS, NON FAT DRY MILK, ASCORBIC ACID, SALT, YEAST, CULTURED WHEAT FLOUR, SOY LECITHIN & NATURAL ENZYMES), CHICKEN ( CHICKEN, WATER, RICE STARCH, SALT), OR TURKEY, CAGE-FREE EGGS (EGGS

Ron Stockman Whole Foods

FDA Food Critical Sep 19, 2012

Knowlan's Club Salad Base, 8 lb.,10 733147 10201 5

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Our Own Fettuccine Pasta Salad, lb., 0 11596 52150

Garden-Fresh Foods, Inc.

FDA Food Critical Sep 19, 2012

Ready Pac super fruit medley Net Wt 10.5 OZ (298g) Dist. by Ready Pac Foods, Inc., Irwindale, CA 91706 USA 1-800-800-7822 www.readypac.com On or before August 16; UPC 7774523746

Missa Bay, LLC

FDA Food Critical Sep 19, 2012

Garden-Fresh Tomato Mozzarella Salad Kit 4 lbs. 0 11596 55163 0

Garden-Fresh Foods, Inc.

FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Knee System is intended for use as a primary or revision total knee replacement.

Omni Life Science

FDA Devices Moderate Sep 19, 2012

Enduramesh Corpectomy Spacer System Product Usage: The Enduramesh is a vertebral body replacement system intended for use in the thoracic and lumbar spine (T1-S1) to replace a collapsed, damaged or unstable vertebral body due to tumor or trauma/fracture. The device is intended for use with either allograft or autograft. The device may be used with a cleared supplemental fixation system based on surgeon discretion and preference.

Lucero Medical LLC

FDA Devices Moderate Sep 19, 2012

CARTO 3 V1.05(FG-5400-00). The CARTO 3 V1.05 System is intended for catheter-based atrial and ventricular mapping. The mapping system allows real-time display of cardiac maps in a number of different formats. Maps may be displayed as cardiac electrical activation maps, cardiac electrical propagation maps, cardiac electrical potential maps, impedance maps and cardiac chamber geometry maps. The acquired patient signals, including body surface ECG and intracardiac electrograms may also be displa

Biosense Webster, Inc.

FDA Devices Moderate Sep 19, 2012

Capsule Neuron Docking Station, a component in the DataCaptor Connectivity System Catalog Number DC-NU-DS-CK The Capsule Neuron Docking Station is a component in the DataCaptor Connectivity System. The Capsule Neuron Docking Station provides connection for the Capsule Neuron UMPC which is a bedside device that enables automatic collection of vital signs data that can connect to the hospital network through a wired Ethernet connection or via a standard 802.11 b/g/n wireless network.

Capsule Tech Inc.

FDA Devices Moderate Sep 19, 2012

Safety monitor included with System 8000 Base The Sarns" Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who is experienced in the operation of this or similar equipment. The safety monitor is indicated to warn when the blood level in the reservoir reaches the operator-set limit, and to stop the arteria

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. The Apex Knee System is intended for use as a primary or revision total knee replacement.

Omni Life Science

FDA Devices Moderate Sep 19, 2012

Multileaf Collimator To be used for single or multiple fractions, delivered as static and/or dynamic beams of radiation, in all areas of the body where such treatment is indicated.

Elekta, Inc.

FDA Devices Moderate Sep 19, 2012

Philips HeartStart MRx monitor/defibrillators Models: M3535A and M3536A, M3536J, M3536M, M3536MC, M3536M1, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6 The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician

Philips Healthcare Inc.

FDA Devices Moderate Sep 19, 2012

CMS-2890 Custom Needle Local Tray containing PVP Prep Pad The PV contained in the kit is used in skin prep

Custom Medical Specialties, Inc.

FDA Devices Moderate Sep 19, 2012

Bard Foley procedural trays packaged in breather bags. The product is packaged ten units in each shipper box, and are sold sterile for single use. Used to catheterize patients. The finished trays are sold in Tyvek breather bags.

C.R. Bard, Inc., Urological Division

FDA Devices Moderate Sep 19, 2012

Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 19, 2012

Optima XR220amx Mobile general purpose radiographic imaging of the human head and body.

GE Healthcare, LLC

FDA Devices Moderate Sep 19, 2012

Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces REF 8253410 (Neuro). LABELING: Box Label: REF 8253410 x1***NIM-Response 3.0 Patient Interface***Medtronic Xomed, Inc., 6743 Southpoint Drive North Jacksonville, FL 32216-0980 USA***Rx Only***Lot***SN:***" Top of unit is labeled in part: "***NIM-Response 3.0***Medtronic***" Bottom/Underside of unit is labeled in part: "***5X20mm FA.L., 32mA. 250VAC***REF***MEDTRONIC XOMED INC. JACKSONVIL

Medtronic Xomed, Inc.

FDA Devices Low Sep 19, 2012

BLOM-SINGER indwelling TEP Occluder, catalog IN2004-TO The Blom-Singer Indwelling (TEP(tracheoesophageal Puncture) Occluder is a non-valved silicone prosthesis designed for placement in and maintenance of the TE (tracheoesophageal) puncture following total laryngectomy. The Blom-Singer Indwelling TEP (tracheoesophageal Puncture) Occluder is indicated for placement in and maintenance of the TE puncture following total laryngectomy when placement, or replacement, of an indwelling prosthesis is

Helix Medical LLC

FDA Devices Moderate Sep 19, 2012

Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces 8253200 (Response) LABELING: Box Label: REF 8253200 x1***NIM-Response 3.0 Patient Interface***Medtronic Xomed, Inc., 6743 Southpoint Drive North Jacksonville, FL 32216-0980 USA***Rx Only***Lot***SN:***" Top of unit is labeled in part: "***NIM-Response 3.0***Medtronic***" Bottom/Underside of unit is labeled in part: "***5X20mm FA.L., 32mA. 250VAC***REF***MEDTRONIC XOMED INC. JACKSONVILLE

Medtronic Xomed, Inc.

FDA Devices Moderate Sep 19, 2012

CMS-4219-R2 Custom Laser Pack containing 2 oz bottles PVP Prep Solution The PV contained in the kit is used in skin prep

Custom Medical Specialties, Inc.

FDA Devices Moderate Sep 19, 2012

Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T, ST241T, ST242T, ST243T, ST244T, and ST245T). The S4 Spinal System is intended for anterior/anterolateral and posterior, non-cervical pedicle and non-pedicle fixation. Fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion using autograft or allograft. The device is indicated for treatment of the following acute and chronic instabilities or deformities: 1 - degenerative disc disease, 2 - spondylol

Aesculap Implant Systems LLC

FDA Devices Moderate Sep 19, 2012

GE Healthcare, Innova 2121IQ, Innova 3131IQ Cardiovascular X-ray imaging systems. K060259: The Innova 3131IQ (3131-IQ) and 2121 IQ (2121-IQ) biplane systems are indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally, rotational angiography procedures. They are also indicated for generating fluoroscopic images of human anatomy for cardiology, diagnostic, and interventional procedures. They are intend

GE Healthcare, LLC

FDA Devices Moderate Sep 19, 2012

Sunquest Laboratory Sunquest Laboratory is intended for use by professionals working in a clinical laboratory. Sunquest Laboratory is intended for use only by professionals who have received extensive training in the use of the software. Sunquest Laboratory is controlled via userdefined security levels, which allow the laboratories to manage data security and integrity. The system is marketed as an automated solution for managing laboratory processes, including: " Patient registration " Order

Sunquest Information Systems, Inc.

FDA Devices Moderate Sep 19, 2012

SUN|DASH RADIUS 252 tanning system; 52 lamps, Ultraviolet Radiation. The device is intended to be used for tanning of the human skin.

JK Products & Services, Inc

FDA Devices Moderate Sep 19, 2012

REF 101-05-30***NOVATION MODULAR DRILL BIT LENGTH: 30mm, DIAMETER 3.2mm***Use with 30mm Screw***STERILE***EXACTECH 2320 NW 56th Court, Gainesville, FL 32653***. To assist the surgeon in the implantation of Novation Hip system components in according to a conventional technique for hemi & total hip arthroplasty. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.

Exactech, Inc.

FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. The Apex Knee System is intended for use as a primary or revision total knee replacement.

Omni Life Science

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.