PlainRecalls

2012 Recalls

3,552 recalls · Page 56 of 72

2012 Recall Year Insight

Federal agencies issued 3,552 product recalls indexed by PlainRecalls in calendar year 2012. That represents about 4.23% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 9.7 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 72 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 9 critical, 35 moderate, and 6 lower-severity recalls. The page references 38 distinct recalling firms operating in 7 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (29), FDA Drug (8), FDA Food (6), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

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 Co…

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: …

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…

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 S…

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…

OrthoPediatrics Corp

CPSC Moderate Aug 1, 2012

Stage and Riser Caddies Recalled by Midwest Folding Products Due to Risk of Injury or Death Child died when stage stored on caddy fell on her

Midwest Folding Products, of Chicago, Ill.

NHTSA Critical Aug 1, 2012

MITSUBISHI 2012: AIR BAGS:FRONTAL:SENSOR/CONTROL MODULE-INACTIVE

MITSUBISHI

CPSC Moderate Jul 31, 2012

Green Toys Recalls Mini Vehicles Due To Choking Hazard

Green Toys Inc., of Mill Valley, Calif.

CPSC Moderate Jul 31, 2012

Liberty Mountain Recalls VAUDE Kenta Child Carriers Due to Fall Hazard

VAUDE Sport GmbH & Company KG, of Germany

NHTSA Critical Jul 27, 2012

MAZDA 2001-2008: ENGINE AND ENGINE COOLING

MAZDA

CPSC Moderate Jul 26, 2012

Motion Sensing Security Lights Recalled by HeathCo due to Electrical Shock Hazard Sold Exclusively at Home Depot

HeathCo LLC, of Bowling Green, Ky.

NHTSA Critical Jul 26, 2012

FORD 2001-2004: ENGINE AND ENGINE COOLING

FORD

FDA Food Critical Jul 25, 2012

Probitotic Dietary Supplement. : iFlora¿ Kids Multi-Probiotic¿

Nutri-Health Supplements Llc.

FDA Food Moderate Jul 25, 2012

Abbott Acres, Meal Pals, Zesty Bean Dip, Ingredients: water, pinto beans, soybean oil, tomato paste, less than 2% sugar, , salt jalapeno peppers, deh…

Old Fashioned Foods, Inc.

FDA Food Critical Jul 25, 2012

SP Standard Process, Cataplex C, Dietary Supplement, (Product # 1650 and 1655) , 90 & 360 Tablets, Proprietary Blend: Veal bone PMG extract, bovine …

Standard Process, Inc.

FDA Food Moderate Jul 25, 2012

Old Fashioned Foods, Jalapeno Bean Dip, Ingredients: water, pinto beans, partially hydrogenated soybean oil, red bell pepper, jalapeno peppers, salt…

Old Fashioned Foods, Inc.

FDA Food Critical Jul 25, 2012

SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend: Dried buckwheat ( leaf) juice,…

Standard Process, Inc.

FDA Food Critical Jul 25, 2012

Standard Process, Pancreatrophin PMG (Product # 6650), 90 Tablets, Proprietary Blend: Bovine pancreas PMG extract, dried alfalfa (whole plant) juice,…

Standard Process, Inc.

FDA Drug Low Jul 25, 2012

HYDROXYZINE HYDROCHLORIDE ORAL SOLUTION, USP, 10 mg/5 mL, 1 PINT (473 mL) bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811…

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

FDA Drug Low Jul 25, 2012

Midol Complete, Acetaminophen, Caffeine, Pyrilamine Maleate, Gelcaps 24 ct. blister, OTC, Distributed by Bayer Health Care, Morristown, NJ 07962 N…

Bayer Healthcare, LLC

FDA Drug Low Jul 25, 2012

Pitocin (Oxytocin Injection, USP) Synthetic 10 units per mL 10 mL, Rx only, Manufactured and Distributed by: JHP Pharmaceuticals, LLC Rochester, MI 4…

JHP Pharmaceuticals, LLC

FDA Drug Critical Jul 25, 2012

Morphine Sulfate Injection, USP, 4mg/mL, 1 mL fill in 2.5 mL Carpuject Cartridge Unit with Luer Lock, packaged 10 Carpujects/carton, CII, Rx only, H…

Hospira Inc.

FDA Drug Moderate Jul 25, 2012

Prefera OB One Gel Capsules, 30 softgels, Rx Only, Manufactured by: IVC industries, Inc. Irving ton, NJ 07111, For: Alaven Pharmaceutical LLC Mariett…

Meda Pharmaceuticals Inc.

FDA Drug Low Jul 25, 2012

Midol Complete, Acetaminophen, Caffeine, Pyrilamine Maleate, Caplets, OTC, a) 16 ct. blister (NDC 0280-8005-16), b)24 ct. blister, Distributed by Bay…

Bayer Healthcare, LLC

FDA Drug Moderate Jul 25, 2012

Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For IV and IC Use after Dilution, Rx Only, American Regent, Inc.…

Luitpold Pharmaceuticals, Inc.

FDA Drug Low Jul 25, 2012

Ciprofloxacin Tablets, USP, 500 mg, Rx Only, 100 Tablets per Bottle, Manufactured in India by: Unique Pharmaceutical Laboratories (A Division of J.B.…

Pack Pharmaceuticals

FDA Devices Moderate Jul 25, 2012

GE Healthcare, Invasive Blood Pressure Care Cables. Product ID Number: 2016995-001, 2016995-002, 2016995-003, 2016995-004.

GE Healthcare, LLC

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 9000, 115V with color screen. The Sarns Perfusion System 9000 is indicated for use as a heart-lung system for pumpi…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Etac¿ Ono Walker, Etac¿ Avant Walker, and Etac¿ Salsa Walker. These products are four-wheeled walkers intended as a walking aid for indoor and ou…

Etac Supply Center Ab

FDA Devices Moderate Jul 25, 2012

Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Z.1 Marticot-33610-Cestas -France +33 (0) 5.57.97.06.30 http;//www.stry…

Stryker Spine

FDA Devices Low Jul 25, 2012

SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software. Product Usage: A customized in-house library of all IV and epidural drug…

Sigma

FDA Devices Critical Jul 25, 2012

CareFusion EnVe Ventilator Designed for use on patients who require respiratory support or mechanical ventilation and weigh a minimum of 5 kg (11 …

CareFusion 203, Inc.

FDA Devices Moderate Jul 25, 2012

Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments are intended for use in laparoscopi…

Integra Limited

FDA Devices Moderate Jul 25, 2012

Stryker T2 Arthrodesis Nailing System. Manufacturer: Stryker Trauma GmbH, Professor-Kuntscher-Str. 1-5, 24232 Schonkirchen Germany. Distributed in …

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Jul 25, 2012

Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX. "Instructions For Use" (QF7.5.1A.R01 thru QF7.5.1A.R06 Care and Handling of Bip…

Stingray Surgical Products, LLC

FDA Devices Moderate Jul 25, 2012

LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotracheal tube or…

LMA North America Inc

FDA Devices Moderate Jul 25, 2012

OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, OEC 9800 MD Motorized C-arm System designed to provide fluoroscopic and spot-film imaging of the p…

GE OEC Medical Systems, Inc

FDA Devices Moderate Jul 25, 2012

Terumo Advanced Perfusion System 1 System 1 Base, 100/120V. The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 hours on th…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

Hudson RCI Concha Therm Neptune Humidifier, Rx Only, Product Usage: Usage: Device that is intended to add moisture to, and sometime to warm, th…

Teleflex Medical

FDA Devices Moderate Jul 25, 2012

Sarns Modular Perfusion System 8000 base, 4 pump 220/240V. The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the e…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

OEC 9900 Elite, OEC 9900 Elite MD Motorized C-arm System, OEC 9900 Elite NAV used as an aid to locate anatomical structures during open or percutaneo…

GE OEC Medical Systems, Inc

FDA Devices Moderate Jul 25, 2012

Terumo Advanced Perfusion System 1 System 1 Base, 220/240V. The Terumo Advanced Perfusion System 1 is indicated for use for up to 6 hours on th…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 25, 2012

EkoSonic MACH4 Endovascular Device (Catalog #500-55106, 500-55112; 500-55118; 500-55124; 500-55130; 500-55140; 500-55150; 500-54106; 500-56130; 500-5…

EKOS Corporation

FDA Devices Moderate Jul 25, 2012

Varian brand Varian Eclipse Treatment Planning System for radiotherapy; Model Number: H48; Product is manufactured and distributed by Varian Medical…

Varian Medical Systems, Inc. Oncology Systems

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…

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 Aler…

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 extra…

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 circula…

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 a…

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 extr…

Terumo Cardiovascular Systems Corporation

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: CPSC + NHTSA + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2012