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, 38 moderate, and 1 lower-severity recalls. The page references 31 distinct recalling firms operating in 7 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (28), CPSC (9), FDA Food (9), 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 Sep 5, 2012

Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle with Extended Insulation 2.75 (6.99cm) Length***Reorder: ES0013M***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0013M -- Lot # 042209-02 Product Usage: Intended for cutting and coagulation of soft tissue.

Unimed Surgical Products, Inc.

FDA Devices Moderate Sep 5, 2012

EXCELART Vantage, Atlas, and Titan MRI Systems, MRT-1503 and MRT-1504. Imaging of the Whole Body, Fluid Visualization, 2D/3D Imaging, MR Angiography/MR Vascular Imaging, Blood Oxygenation Level Dependent Imaging, Perfusion I Diffusion Imaging, and Proton Spectroscopy.

Toshiba American Medical Systems Inc

FDA Devices Moderate Sep 5, 2012

Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry

Sunquest Information Systems, Inc.

FDA Devices Moderate Sep 5, 2012

Toshiba CT systems, Asteion and Aquilion, that are equipped with a PC based computer, or to those older systems (SGI based) that received an improved table by an upgrade purchase. This device is designed to produce cross-sectional images of a human body by reconstruction of xray transmission data from the same axial plane taken at different angles. These images have been proven to be clinically useful in the diagnosis of spine and head injuries, intracranial tumors, blood clots in the brain,

Toshiba American Medical Systems Inc

FDA Devices Moderate Sep 5, 2012

Sunquest Laboratory LabAccess Results Workstation (LARS)

Sunquest Information Systems, Inc.

FDA Devices Moderate Sep 5, 2012

QKC1692E The QKC1692E Quick Connect device connects endoscopes to the sterilization tray for C1220E liquid chemical sterilization processor.

Steris Corporation

FDA Devices Moderate Sep 5, 2012

Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with Extended Insulation 6.5 (16.51cm) Length***Reorder: ES0014M***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0014M-- Lot # 050609-05, 052909-05, 062309-04. Product Usage: Intended for cutting and coagula

Unimed Surgical Products, Inc.

FDA Devices Moderate Sep 5, 2012

The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel, rechargeable, multi-program system that allows the connection of one or two leads with 4, 8, and 16 electrode leads. Product Usage: The Eon and Eon Mini Neurostimulation Systems are indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, intractable low back and leg pain.

Advanced Neuromodulation Systems Inc.

FDA Devices Moderate Sep 5, 2012

Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory Packs (also commonly known as convenience kits and custom procedure trays) are an assembly of medical devices packaged together according to the customer specifications, which are then wrapped in a sterilization wrap and sterilized. This allows the customer to open one package for a surgical procedure instead of many individual packages.

SRI Surgical

FDA Devices Moderate Sep 5, 2012

Product is labeled in part: "***MEDLINE***Extended PTFE Needle 6.5" (16.51cm) Length***Reorder: ES0016***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0016 -- Lot #: 030608-01 and 121808-19. Product Usage: Intended for cutting and coagulation of soft tissue.

Unimed Surgical Products, Inc.

FDA Devices Moderate Sep 5, 2012

CaviCide, Part Numbers: 13-1025, 13-1000, 13-1024, MC-1000. Alternate brands: EnviroCide, part number: 13-3325. Private labeled products of Cavicide: Backscratchers Cavicide, part number: 13-4800. MaxiSpray Plus, part numbers: 13-7400 and 13-7405. pdCARE Surface Disinfectant, part numbers: 13-7525 and 13-7500. Z3 Surface Disinfectant, part number: 13-7900. CaviCide is a multi-purpose disinfectant/decontaminant cleaner for use on hard, non-porous inanimate surfaces. CaviCide is

Metrex Research, LLC.

FDA Devices Moderate Sep 5, 2012

Canon Solid State X-ray Imager (Flat Panel/Digital Imager), Digital Radiography, Models CXDI-55C, CXDI-55G and CXDI-70C. These devices are intended to replace radiographic film/screen systems in all general purpose diagnostic procedures.

Canon Inc.

FDA Devices Moderate Sep 5, 2012

V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for Use for the V Series include the monitoring of the following human physiological parameters: ECG waveform derived from 3, 5, 6 and 12 lead measurements; Heart Rate; Pulse Oximetry (SpO2); ST Segment Analysis; Arrhythmia Detection; Non Invasive Blood Pressure (NIBP); Invasive Blood Pressur

Mindray DS USA, Inc. d.b.a. Mindray North America

FDA Devices Moderate Sep 5, 2012

Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle with Extended Insulation 4.0" (10.16cm) Length***Reorder: ES0016AM***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0016AM -- Lot #: 062408-08, 062509-01. Product Usage: Intended for cutting and coagulation

Unimed Surgical Products, Inc.

FDA Devices Low Sep 5, 2012

Mini-Infuser Model 300XL Multispeed Infusion Pump, an Rx battery operated syringe infusion pump with an active time scale and rate selector switch; product codes 2M8171 and 2M8171R. Product Usage: These product codes includes refurbished units. Intended for the controlled rate delivery of small volume parental fluids as prescribed by a physician. Usage: The Mini-Infuser System is designed for controlled intermittent administration of intravenous medication.

Baxter Healthcare Corp.

FDA Devices Moderate Sep 5, 2012

DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Electrode Kits (containing DGPHP RFA High-Power single use grounding pads) The product is used during ablation surgical procedures.

Nellcor Puritan Bennett Inc. (dba Covidien LP)

FDA Devices Moderate Sep 5, 2012

Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade 6.5 (16.51cm) Length***Reorder: ES0014***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0014 -- Lot # 042209-03. Product Usage: Intended for cutting and coagulation of soft tissue.

Unimed Surgical Products, Inc.

FDA Devices Moderate Sep 5, 2012

Whole Body X--ray Scanner This device is indicated as a whole body volume CT system. The system produces volumes of up to 320 axial slices in a single rotation.

Toshiba American Medical Systems Inc

FDA Devices Moderate Sep 5, 2012

syngo.plaza, Model number 10592457. Intended use: radiological image processing system.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 5, 2012

TRESTLE LUXE¿ Anterior Cervical Plating System, Product code KWQ. 510(k) K102820. The TRESTLE LUXE Anterior Cervical Plating System is a temporary device used to stabilize the cervical spine during bone fusion development. Device implants include a range of plate sizes and bone screws to provide the versatility required for the specific indications noted. Fixation is achieved by means of a rigid plate that is surgically attached to the spine with bone screws. The TRESTLE LUXE Anterior Cervica

Alphatec Spine, Inc.

FDA Devices Critical Sep 5, 2012

ON-Q pump with ONDEMAND bolus button, ON-Q C-bloc with ONDEMAND; ON-Q C-bloc with Select a Flow and ONDEMAND Model/Reference #: 7000180, 7000181, 7000182, 7000367, 7000397, CB003, CB005, CB006, P400X1-7+5/60, P400X2-14+5/30, P400X5+5/60, and PMB01. Part Numbers: 101347100, 101347300, 101347400, 101360200, 101368400, 101368600, 101368700, 102987000, 102987200, 102987300, 103161800, 103534300, 5001438, 5001470, 5001651, 5001780, 5001808, 5001809, 5001812, 7000180, 7000181, 7000182, & 7000367.

I-Flow Corporation

FDA Devices Moderate Sep 5, 2012

syngo Imaging XS. Radiological image processing system.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 5, 2012

Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed to be connected to 4, 8, or 16 electrode leads or a lead extension. Product Usage: The Eon and Eon Mini Neurostimulation Systems are indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, intractable low back and leg pain.

Advanced Neuromodulation Systems Inc.

FDA Devices Moderate Sep 5, 2012

ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) - pH Blood Gas and Electrolytes Analyzer System. Intended Use The ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) are portable, automated analyzers that measure pH, blood gases, electrolytes, glucose and oximetry (ABL80 FLEX CO-OX only) in whole blood. The ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) analyzer systems are intended for use by trained technologists,

Sendx Medical Inc

FDA Devices Moderate Sep 5, 2012

3DKnee e+ Tibial Insert - HXLPE-VE, Sterile, Material: Highly cross linked vitamin E PE, Sz 2/9mm. The insert is intended to more closely match the kinematics of the knee, allowing some rotation along the medial condyle and increased congruency along lateral condyle. This insert is to be used along with the other components that comprise the 3DKnee System.

Encore Medical, Lp

FDA Devices Moderate Sep 5, 2012

Product is labeled in part: "***MEDLINE***Extended 5mm PTFE Coated Ball 5.0 (12.70cm) Length***Reorder: ES0009***Contents: 1 Each***SINGLE USE ONLY**latexfree***RX Only***STERILE EO***www.medline.com Manufactured for Medline Industries, Inc. MEDLINE is a registered trademark of Medline Industries, Inc. 1-800-MEDLINE***Mundelein, IL 60060 USA Made in USA.***" Part # ES0009 -- Lot # 052709-01 Product Usage: Intended for cutting and coagulation of soft tissue.

Unimed Surgical Products, Inc.

FDA Devices Critical Sep 5, 2012

OEC IT3000; IT2500 (EnTrak); IT2500 Plus (EnTrak Plus); IT3500 (InstaTrak); IT3500 Plus (InstaTrak Plus); ConneCTstat; and ConneCTstat Plus picture archiving and communications systems. The systems are an aid to locate anatomical structures during open or percutaneous surgical procedures. It is intended for use in medical conditions that may benefit from the use of stereotactic surgical technique. The system provides a reference to rigid anatomical structures such as sinus, skull, long bone,

GE OEC Medical Systems, Inc

FDA Devices Moderate Sep 5, 2012

Apelo Modular Screwdriver labeled in part: "APELO PEDICLE SCREW SYSTEM***Modular Screwdriver***Atlas Spine, Inc.***www.AtlasSpine.com*** 1555 Jupiter Park Drive #4***Jupiter, Florida 33458***561-741-1108***Tissue Sleeve***MFG Date: XX/XX/XXXX***Lot #: XXXX***Weldment***MFG Date: 03/23/2009***Sleeve Assembly***MFG Date: XX/XX/XXXX***Lot #: XXXX***Qty: 1 Rx Only***Non-Sterile. Sterilize Prior to Use*** Rev. A***. The Modular Screwdriver is used to insert modular pedicle screw implants which are

Atlas Spine, Inc.

NHTSA No agency class Sep 5, 2012

HONDA 2007-2011: ELECTRICAL SYSTEM:WIRING

HONDA

NHTSA No agency class Sep 5, 2012

HONDA 2012: AIR BAGS:ON-OFF SWITCH ASSEMBLY

HONDA

NHTSA No agency class Sep 4, 2012

FORD 2013: ENGINE AND ENGINE COOLING

FORD

NHTSA No agency class Sep 4, 2012

LAMBORGHINI 2004-2006: STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS

LAMBORGHINI

CPSC No agency class Aug 30, 2012

Avalanche Airbags Recalled by Snowpulse Due to Risk of Injury1

Snowpulse SA, of Martigny, Switzerland

CPSC No agency class Aug 30, 2012

BatteriesPlus Expands Recall of Battery Packs Used with Cordless Tools Due to Explosion Hazard

CPSC No agency class Aug 30, 2012

Cost Plus Recalls Silk Floor Mats Due to Laceration Hazard; Sold Exclusively at Cost Plus World Market

Cost Plus Inc., of Oakland, Calif.

CPSC No agency class Aug 30, 2012

DeVilbiss Air Power Co Recalls Air Compressors Due to Fire Hazard

DeVilbiss Air Power Co. of Jackson, Tenn.

CPSC No agency class Aug 30, 2012

Inflatable Recreational Tubes Recalled by Tractor Supply Due to Chemical Burn and Irritation Hazard

CPSC No agency class Aug 30, 2012

Meijer Stores Recalls Bicycles Due to Fall Hazard

Meijer Inc., of Grand Rapids, Mich.

CPSC No agency class Aug 30, 2012

Mr. Coffee Single Cup Brewers Recalled by JCS Due to Burn Hazard

CPSC No agency class Aug 30, 2012

Shimano Recalls to Repair PRO VIBE Bicycle Handlebars Due to a Fall Hazard

Great Go Cycles Inc., of Taiwan

CPSC No agency class Aug 30, 2012

Specialized Bicycle Components Expands Recall of Bike Brake Levers Due to Crash Hazard

FDA Food Moderate Aug 29, 2012

Pineapple Pies Case Label (side 1) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Cocoa, Coconut, Sugar, Butter, Vanilla, Cornstarch, Eggs Case Label (side 2) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Fruit, Sugar, Butter, Almond, Salt Pie Label: Pineapple

Flywheel's Pies

FDA Food Critical Aug 29, 2012

Processed Yellow Onions - Yellow Slivered

Freshpoint Atlanta, Inc.

FDA Food Moderate Aug 29, 2012

Libby's Gourmet Desserts brand pecan pie. Pies placed in metal pie tins which are then put in a cardboard sleeve with plastic wrapping

Libby's Gourmet Desserts

FDA Food Critical Aug 29, 2012

Processed Yellow Onions - Veg. Asian Bias Mix

Freshpoint Atlanta, Inc.

FDA Food Moderate Aug 29, 2012

Sugar Free Apple Pies Case Label (side 1) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Cocoa, Coconut, Butter, Vanilla, Cornstarch, Eggs Case Label (side 2) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Fruit, Sugar, Butter, Almond, Salt

Flywheel's Pies

FDA Food Critical Aug 29, 2012

Processed Yellow Onions - Veg. Harvest Hash Mix

Freshpoint Atlanta, Inc.

FDA Food Moderate Aug 29, 2012

Sweet Potato Pies Case Label (side 1) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Cocoa, Coconut, Sugar, Butter, Vanilla, Cornstarch, Eggs Case Label (side 2) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Nigeriense: Fruit, Sugar, Butter, Almond, Salt Pie Label: Sweet Potato

Flywheel's Pies

FDA Food Critical Aug 29, 2012

Pine Nuts, 5lbs, Item 40476-214, UPC 8 12986 01288.

Essential Living Foods, Inc

FDA Food Critical Aug 29, 2012

Cool Creations Fajita Mix Deluxe packaged for food service in 5-lb. plastic trays, 4 per case (item #15741).

Cool Creations, LLC

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.