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 33 distinct recalling firms operating in 8 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (27), FDA Food (14), CPSC (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 Jul 25, 2012

Philips Brilliance 6, 16, 40, 64, Big Bore, iCT and iCT SP are Computed Tomography X-Ray Systems. The devices are Computed Tomography Systems that are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 25, 2012

Alere Triage Tox+MTD Drug Screen, PN 94400 Product Usage: The Alere Triage TOX Drug Screen is a fluorescence immunoassay to be used with the Alere Triage Meters for the qualitative determination of the presence of drug and/or the major metabolites above the threshold concentrations of up to 10 distinct drug classes, including assays for acetaminophen/paracetamol, amphetamines, methamphetamines, barbiturates, benzodiazepines, cocaine, methadone, opiates, phencyclidine, THC and tricyclic antid

Alere San Diego, Inc.

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 4 pump 100V. 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Terumo Advanced Perfusion System 1. System 1 base 220/240V. The Terumo Advanced Perfusion System I is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only When used by a qualified perfusionist who is experienced in the operation of Sarns or similar equipment.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

epoc Blood Analysis BGEM Test Cards for use with the epoc(R) Blood Analysis System Product Usage: Usage: epoc Blood Analysis BGEM Test Cards are used with the epoc(R) Blood Analysis System which is a POC testing system

Epocal Inc

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 5 pump 115V. The Sarns Modular Perfusion Systern 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

BD Gram Stain Kit, containing 1- 250 mL bottle of Gram Crystal Violet, and additional reagents: Gram Iodine (Stabilized), Gram Decolorizer, Gram Safranin. Gram Stain Kits and Reagents are used to stain microorganisms from cultures or specimens by the differential Gram method.

Becton Dickinson & Co.

FDA Devices Moderate Jul 25, 2012

Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK, REF 89-6664.04 GEO-MED TOTAL HIP PACK, REF 89-6664.03 surgical kits

DeRoyal Industries Inc

FDA Devices Moderate Jul 25, 2012

Spacelabs Medical Xprezzon Bedside Monitor, Model 91393, installations with Option C. It is a patient monitor with arrhythmia detection or alarms. The Spacelabs Healthcare Xprezzon Bedside Monitor is intended to alert the user to alarm conditions that are reported by Spacelabs Healthcare parameter modules and/or other devices via Flexport interfaces. The patient monitors are also capable of displaying alarm conditions on other monitors that are on the network through the Alarm Watch feature.

Spacelabs Healthcare, Llc

FDA Devices Moderate Jul 25, 2012

System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 5 pump 220/240V. 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 9000, 220/240V with color screen. The Sarns Perfusion System 9000 is indicated for use as a heart-lung system for pumping blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified perfusionist who is experienced in the operation of Sarns or similar equipment.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

OEC 8800 Flexiview designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The OEC 8800 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 ap

GE OEC Medical Systems, Inc

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 4 pump 115V. 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

MicroCool Breathable Impervious Surgical Gown, (Large and X-Large), Sterile, Made in Honduras. The Kimberly Clark Micro COOL Surgical Gowns are sterile single use surgical apparel intended to be worn by heathcare professionals to help protect the patient and the healthcare worker from the transfer of microorganisms, body fluids and particulate matter.

Kimberly-Clark Corporation

FDA Devices Moderate Jul 25, 2012

System 1 Base, 220/240V. The Terumo Advanced Perfusion System 1 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 5 pump 100V. he 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.

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Jul 25, 2012

Infusomat(R) Space Pump (US Version) with software version 686G030103 (commonly termed 'G03'), 686E030003, 686F030005, 686F030007, 686G030002, and 686G030102. Intended for use with adults, pediatrics and neonates and is intended to provide infusions of parenteral fluids/medications, blood and blood products indicated for infusion through FDA approved routes of administration.

B. Braun Medical, Inc.

FDA Devices Moderate Jul 25, 2012

Terumo Advanced Perfusion System 1. System 1 base 100/120V. The Terumo Advanced Perfusion System I is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only When used by a qualified perfusionist who is experienced in the operation of Sarns or similar equipment.

Terumo Cardiovascular Systems Corporation

FDA Devices Low Jul 25, 2012

Presage ST2 Assay, catalog numbers BC-1065 and BC-1065E. The Critical Diagnostics Presage ST2 Assay kit is an in vitro diagnostic device that quantitatively measures ST2 in serum or plasma by enzyme-linked immunosorbent assay (ELISA) in a microtiter plate format. The Presage ST2 Assay is indicated to be used in conjunction with clinical evaluation as an aid in assessing the prognosis of patients diagnosed with chronic heart failure.

Critical Diagnostics

FDA Devices Moderate Jul 25, 2012

GE Healthcare Optima Mobile X-ray System. The GE Automatic Mobile X-Ray (AMX ) Series are intended to take exposures utilizing film or computed radiography ( CR )

GE Healthcare, LLC

FDA Devices Moderate Jul 25, 2012

Gram Crystal Violet 250 mL, catalog #212525, in cartons of 4 bottles. Gram Stain Kits and Reagents are used to stain microorganisms from cultures or specimens by the differential Gram method.

Becton Dickinson & Co.

FDA Devices Moderate Jul 25, 2012

MicroCool Breathable Impervious Gown with Secure Fit Surgical, (Large and X-Large), Made in Honduras. The Kimberly Clark Micro COOL Surgical Gowns are sterile single use surgical apparel intended to be worn by heathcare professionals to help protect the patient and the healthcare worker from the transfer of microorganisms, body fluids and particulate matter.

Kimberly-Clark Corporation

FDA Devices Moderate Jul 25, 2012

Hitachi Scenaria CT System Software Product Usage: The Scenaria system is indicated to acquire axial volumes of the whole body including the head. The images can be acquired in either axial, helical, gated or dynamic modes. The volume datasets acquired by the Scenaria can be post processed by the Scenaria to provide additional information. Post processing capabilities included in the Scenaria software include CT angiography (CTA), Multi-planar reconstruction (MPR) and volume rendering.

Hitachi Medical Systems America Inc

FDA Devices Moderate Jul 25, 2012

Gulf Fiberoptics, Inc.

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 9000, 100V with color screen. The Sarns Perfusion System 9000 is indicated for use as a heart-lung system for pumping blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified perfusionist who is experienced in the operation of Sarns or similar equipment.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Abbott Molecular Bar Code Scanner User's Guide; instructions for setting up the Bar Code Scanner LN 6L89-01, a component of the Abbott m2000 Instrument System; Abbott Molecular Inc., Des Plaines, IL 60018 USA; list number 06L88-02. Language configuration bar codes - Intended Use: The bar code scanner is a hand-held device that provides a convenient means of scanning sample bar codes to allow positive sample identification and is supplementary to the computer keyboard. Both the scanner and the

Abbott Molecular

NHTSA No agency class Jul 25, 2012

HYUNDAI 2007-2009: AIR BAGS:FRONTAL:SENSOR/CONTROL MODULE-INACTIVE

HYUNDAI

CPSC No agency class Jul 24, 2012

Kolcraft Recalls Contours Tandem Strollers Due to Fall and Choking Hazards

CPSC No agency class Jul 24, 2012

Peg Perego Recalls Strollers Due to Risk of Entrapment and Strangulation; One Child Death Reported

NHTSA No agency class Jul 24, 2012

HYUNDAI 2012-2013: AIR BAGS:SIDE/WINDOW

HYUNDAI

CPSC No agency class Jul 19, 2012

Burlington Coat Factory Recalls Power Strips Due to Fire Hazard

Burlington Coat Factory, of Burlington, N.J.

CPSC No agency class Jul 19, 2012

Children's Beach Chairs Recalled by Downeast Concepts Due to Laceration Hazard

Downeast Concepts Inc., dba Backyard and Beyond, of Yarmouth, Maine

CPSC No agency class Jul 19, 2012

Club Car Recalls Golf and Transport Vehicles Due to Fire Hazard

Club Car LLC, of Augusta, Ga.

NHTSA No agency class Jul 19, 2012

INTERNATIONAL 2010: WHEELS

INTERNATIONAL

NHTSA No agency class Jul 19, 2012

ACURA,HONDA 2012-2013: LATCHES/LOCKS/LINKAGES:DOORS:LATCH

ACURA,HONDA

FDA Food Moderate Jul 18, 2012

Kit item #30699-76, includes Mozzarella Sticks, 2.25 oz, 12bags/kit; Cheddar Bacon Skins, 3oz, 24 bags/kit; and Sour Cream & Onion Skins 3oz, 12bags/kit. kit item#30679-11, 30679-12, and 30679-13, includes Mozzarella Sticks 2.25oz, 12bags/kit, Cheddar bacon skins 3oz, 24 bags/kit, and Sour Cream & Onion skins 3oz, 12bags/kit. Kit Item#30845-A- Onion Ring Clip Strip, 2oz, 24 bag/clip strip.

Inventure Foods

FDA Food Moderate Jul 18, 2012

Coca Cola Zero, 20 fl. oz., The Coca Cola Company.

Coca-Cola Refreshments, USA Inc.

FDA Food Low Jul 18, 2012

Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #65

H & L Jerch Sales, Inc.

FDA Food Moderate Jul 18, 2012

IQF Oysters 3lbs, Assi Brand, Item# 20083K,10x3 lb; Oyster Block, Assi Brand, item# 20085K, 30x1 lb; Oysters 8 oz - Tiny, Assi Brand, item# 20086, 40x8 oz; IQF Oysters 20 oz - Tiny, Assi Brand, item#20093, 20x20 oz.

KOREAN FARM, INC.

FDA Food Critical Jul 18, 2012

Light Dry Roasted Unsalted Split Peanuts, Product Code: 400260, packaged in 30 lb. vacuum packed plastic bags placed inside cardboard shipping boxes. The total packaging size is 2100 lbs = 70 x 30 lb boxes.

Pro Nutech Inc.

FDA Food Moderate Jul 18, 2012

Coca Cola Cherry Zero, 20 fl. oz. (1.25 pt), The Coca Cola Company.

Coca-Cola Refreshments USA, Inc.

FDA Food Critical Jul 18, 2012

Medium Chopped Peanut Granules, Product Code #410016, packaged in 30 lb. vacuum packed plastic bags within cardboard shipping boxes. The total packaging size is 2100 lbs = 70 x 30 lb boxes.

Pro Nutech Inc.

FDA Food Moderate Jul 18, 2012

Surasang Chanbada Frozen Oyster I.Q.F (8oz), 40pack/case

Wang Globalnet

FDA Food Moderate Jul 18, 2012

Giusto's Wheat Germ, Raw, Net Wt. 25 lb, (11.34 Kg) paper bag; Item number: 154205 Giusto's 344 Littlefield Ave. South Francisco, CA 94080

Giusto's Specialty Foods LLC

FDA Food Critical Jul 18, 2012

Banner Mountain Sprouts;Alfalfa Broccoli Sprouts; California Certified Organic Sprouts. 100% certified organic seeds used. Sacramento, Ca 95820. Net Wt. 4 oz; Rinse and Eat; Perishable, Keep refrigerated. UPC 4 oz size: 0- 9691172840 9;

Banner Mountain Sprouts Inc

FDA Food Critical Jul 18, 2012

Banner Mountain Sprouts;Alfalfa Sprouts; California Certified Organic Sprouts. 100% certified organic seeds used. Sacramento, Ca 95820. Net Wt. 4 oz; 1 lb and 2 lb packages. Rinse and Eat; Perishable, Keep refrigerated. UPC 4 oz size: 0- 9691172842 3; UPC 1 lb size: 0 96911 72850 8

Banner Mountain Sprouts Inc

FDA Food Critical Jul 18, 2012

Product is labeled in part: "***LEASA Living Alfalfa Sprouts***CHOLESTEROL FREE***PRESERVATIVE FREE***KEEP REFRIGERATED***NET WT. 6 OZ. (168 g)***" Product is packaged in 6 oz clear plastic containers with UPC 75465-55912. UPC Code and expiration date are located on the side of the container.

LEASA Industries Co., Inc.

FDA Food Moderate Jul 18, 2012

Clams, Frozen Boiled Baby, in shell, 10 oz packages, 24 pkgs/carton, item #20699K. UPC 081652 206996.

Rhee Brothers Incorporated

FDA Food Critical Jul 18, 2012

Kroger Fresh Selections Greener Supreme; Iceberg lettuce, Romaine lettuce, Carrots and Red Cabbage; 12 oz plastic bag. Best if used by date: June 19, 2012: UPC 0 11110 91039 4 Distributed by the Kroger Co., Cincinnati, OH 45202

Dole Fresh Vegetables 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.