PlainRecalls

2012 Recalls

3,552 recalls · Page 65 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 14 critical, 31 moderate, and 5 lower-severity recalls. The page references 24 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 (37), FDA Drug (7), CPSC (4), 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 Drug Moderate Jun 27, 2012

Zemplar (paricalcitol) Injection, 5 mcg/mL in 2 mL multi-dose vials, 25 vial carton, Rx only, Manufactured by Hospira, Inc. For Abbott Laboratories, …

Abbott Laboratories

FDA Drug Critical Jun 27, 2012

Morphine Sulfate Extended Release tablet, 30 mg, 60 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, Ok 74146-6234, NDC 54868-4033-00

Physicians Total Care, Inc

FDA Drug Critical Jun 27, 2012

Morphine Sulfate Immediate Release tablet, 30 mg/120 tablet bottles, Rx only, Physician Total Care, Inc, Tulsa, OK 74146-6234, NDC 54868-4973-00

Physicians Total Care, Inc

FDA Drug Moderate Jun 27, 2012

Lipitor (Atorvastatin calcium); 40 mg, 30 TABLETS, Rx only, Repacked & distributed: Physicians Total Care, Inc., Tulsa OK 74146, NDC 54868-4229-0

Physicians Total Care, Inc.

FDA Drug Moderate Jun 27, 2012

Hands Down Medicated Lotion Soap, 1 gallon bottle, 4 gallons per case, Distributed by PCS Industries, Crestwood, IL, 60446

Kutol Products Co Inc

FDA Drug Low Jun 27, 2012

Jolessa (levonorgestrel/ethinyl estradiol tablets, USP) 0.15 mg/0.03 mg, each Dispenser contains 91 tablets, 91 Day Regimen, Rx Only, Shaping Women's…

Teva Pharmaceuticals USA, Inc.

FDA Drug Moderate Jun 27, 2012

LifeGas OXYGEN COMPRESSED UN1072 USP, Distributed by: Linde

Linde Gas LLC

FDA Devices Moderate Jun 27, 2012

TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal System is an ultrasonic aspirator that emulsifies and removes soft tissue. The TX1 …

American Optisurgical Inc

FDA Devices Low Jun 27, 2012

PrepStain GYN 480 Disposable Test Kit with PreCoat Slides (Catalog #490523

Tripath Imaging, Inc.

FDA Devices Moderate Jun 27, 2012

Implant, Dental, Endosseous, Acid Etched, ICE, Osseotite, Internal Connection. . Product is labeled in part: "***Certain 3.25, 13***REF IOSM313…

Biomet 3i, LLC

FDA Devices Moderate Jun 27, 2012

VerifyNow P2Y12 Assay, Part Number: 85064, All reagent lots. Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the l…

Accumetrics Inc

FDA Devices Moderate Jun 27, 2012

SARNS FLEXIBLE ARTERIAL CANNULA: 7.3 MM (22 FR) 00 WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is …

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Jun 27, 2012

NIDEK Medical M5C5/ MARK5 NUVO/STD, 230 V~50/60 Hz - 420 W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

SARNS HIGH-FLOW AORTIC ARCH CANNULA: 5.2 MM (16 FR) 00 WITH 3/8" CONNECTOR, 7.5" (19 CM) LONG. The Sarns High Flow Aortic Arch Cannula is indicate…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 27, 2012

SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is ind…

Terumo Cardiovascular Systems Corporation

FDA Devices Low Jun 27, 2012

PrepStain Syringing Pipettes 240 (Catalog #490517)

Tripath Imaging, Inc.

FDA Devices Moderate Jun 27, 2012

24FR FLEX ART CANN NON STERILE. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopul…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 27, 2012

SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR, 11" (28 CM) LONG. The Sarns High Flow Aortic Arch Cannula is indicated…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 27, 2012

SARNS FLEXIBLE ARTERIAL CANNULA: 8.0 MM (24 FR) 00 WITH 3/8" CONNECTOR, CM MARKING, 10" (25 CM) LONG. The Sarns High Flow Aortic Arch Cannula is i…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 27, 2012

Boston Scientific Profile Single-Use Pediatric Snare 13mm UPN Outer Box: M00562551 Inner Pouch: M00562550 The single-use Profile Polypectomy Sn…

Boston Scientific Corporation

FDA Devices Critical Jun 27, 2012

GE Healthcare, Aestiva/5 7900 SmartVent, anesthesia machine. Used in Datex-Ohmeda Aestiva/5 Anesthesia Systems.

GE Healthcare, LLC

FDA Devices Critical Jun 27, 2012

NIDEK Medical MARK5 NUVO 8 /OCSI, 230 V~50/60Hz - 420 W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

SARNS HIGH-FLOW AORTIC ARCH CANNULA: 6.5 MM (20 FR) 00 WITH 3/8" CONNECTOR, 11" (28 CM) LONG, WITH XCOATING SURFACE COATING. The Sarns High Flow A…

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Jun 27, 2012

NIDEK Medical MARK5 NUVO 8 STD, 115 V~60Hz - 500W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and gener…

Non-Invasive Monitoring Systems, Inc.

FDA Devices Moderate Jun 27, 2012

Boston Scientific Profile Single-Use Pediatric Snare 11mm UPN Outer Box M00562531 Inner Pouch: M00562530 , The single-use Profile Polypectomy S…

Boston Scientific Corporation

FDA Devices Critical Jun 27, 2012

NIDEK Medical NUVO LITE MODEL 925 OCSI, 3LPM 230V - 60Hz - 280W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

Philips Multi Diagnost Eleva II with swivel cable Product Codes; 708032, 708036 Multi Diagnost Eleva with FlatDetector with swivel cable Product …

Philips Healthcare Inc.

FDA Devices Critical Jun 27, 2012

NIDEK Medical M5C5/ MARK5 NUVO/OCSI, 230 V~50/60 Hz -420 W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

Boston Scientific Profile Single-Use Pediatric Snare 27mm UPN Outer Box: M00562571 Inner Pouch: M00562570 The single-use Profile Polypectomy Sn…

Boston Scientific Corporation

FDA Devices Moderate Jun 27, 2012

Philips Digital Diagnost Software, software release 2.0.2 and 2.0.2SP1 including mirror icon Stationary Fluoroscopic system

Philips Healthcare Inc.

FDA Devices Critical Jun 27, 2012

NIDEK Medical NUVO LITE MODEL 525 OCSI, 115V -60Hz - 330W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Critical Jun 27, 2012

NIDEK Medical MARK5 NUVO / M5C5, 115 V ~60Hz - 410 W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

Stryker Howmedica Osteonics Accolade Offset Rasp Handle Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA Stryker France ZAC Satol…

Stryker Howmedica Osteonics Corp.

FDA Devices Critical Jun 27, 2012

NIDEK Medical NUVO LITE MODEL 925 OCSI, 230V - 50Hz - 300W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

VerifyNow System, part #85005-6H Product Usage: The VerifyNow P2Y12 assay device is a whole blood assay used in the laboratory or point of care s…

Accumetrics Inc

FDA Devices Moderate Jun 27, 2012

Covidien ROTICULATOR 55-4.8 Single Use Stapler REF# 017614 The RETICULA TOR TM Single Use Staplers have applications in abdominal, gynecologic a…

Covidien LP

FDA Devices Moderate Jun 27, 2012

The product is Pathfinder SL, version 1.6.0.3057 software used with the Spacelabs Healthcare Pathfinder SL Holter Analyzer, version 1.6.0. Product…

Spacelabs Healthcare, Llc

FDA Devices Moderate Jun 27, 2012

SARNS FLEXIBLE ARTERIAL CANNULA: 6.7 MM (20 FR) 00 WITH 3/8" CONNECTOR,SUTURE RING, 9.5" (24 CM) LONG. The Sarns High Flow Aortic Arch Cannula is …

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 27, 2012

Covidien ROTICULATOR 55-3.5 Single Use Stapler REF# 017612 The RETICULA TOR TM Single Use Staplers have applications in abdominal, gynecologic an…

Covidien LP

FDA Devices Low Jun 27, 2012

PrepStain GN 480 Disposable Kit Catalog/Model 490542 This is a complete kit, per the firm's explanation, that contains the PrepStain Syringing Pipet…

Tripath Imaging, Inc.

FDA Devices Low Jun 27, 2012

PrepStain Installation Kit (PreCoat), Catalog/Model # 490528

Tripath Imaging, Inc.

FDA Devices Critical Jun 27, 2012

NIDEK Medical NUVO LITE MODEL 520 STD, 115V - 60Hz - 330W. Oxygen Concentrator.

Nidek Medical Products Inc

FDA Devices Moderate Jun 27, 2012

CPB CATHETER KIT- DR.VAN TRIGHT. The Sarns High Flow Aortic Arch Cannula is indicated for use in perfusion of the ascending aorta during cardiopul…

Terumo Cardiovascular Systems Corporation

CPSC Moderate Jun 27, 2012

Alltrade Tools Recalls Kawasaki Cordless Drill Due to Burn Hazard; Sold Exclusively at Costco

Wuxi Xinju Electric Tools Co., Ltd. of Wuxi, China

CPSC Moderate Jun 27, 2012

Big Cat Human Powered Vehicles Recalls Bicycle Due to Crash Hazard

Big Cat Human Powered Vehicles LLC, of Winter Garden, Fla.

CPSC Moderate Jun 27, 2012

Samuel Lawrence Furniture Recalls Sleigh Beds Due to Fall Hazard

Poh Huat Furniture Ind., of Malaysia

CPSC Moderate Jun 26, 2012

Servpro Recalls Notus Air Movers Due to Fire Hazard

EDIC, of Los Angeles, Calif.

NHTSA Critical Jun 22, 2012

CHEVROLET 2011-2012: FUEL SYSTEM, GASOLINE:STORAGE:TANK ASSEMBLY:MOUNTING

CHEVROLET

NHTSA Critical Jun 22, 2012

CHEVROLET 2011-2012: ENGINE AND ENGINE COOLING

CHEVROLET

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