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 5 critical, 44 moderate, and 1 lower-severity recalls. The page references 19 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (20), FDA Drug (17), FDA Devices (13), 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 Moderate Dec 12, 2012

Zingerman's Bakehouse, Inc.

FDA Food Critical Dec 12, 2012

Colby , Sizes could be 8 oz, 5lbs, 10lb, or 25lbs- vacuum packed

Kennys Farmhouse Cheese

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Chocolate Chess Pie

Zingerman's Bakehouse, Inc.

FDA Food Critical Dec 12, 2012

Sara Lee Butter Streusel Coffee Cake, Net Wt. 11.5 oz ; 8 cakes per 5.75 lb case; Distributed by Sara Lee Corp., Downers Grove, IL 60515 U.S.A.; UPC: 032100023429

Hillshire Brands Company

FDA Food Critical Dec 12, 2012

Serano Gelato Chocolate Peanut Butter, 16 oz, contained in a semiflexible paper container, manufactured by Fresca Foods, CO.

Boulder Ice Cream

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Almond Pound Cake Net wt. 1.25 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Orange-Almond Magic Brownies 1/4 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Sourcream Coffeecake Net wt. 3 LB; 1.25 LB

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Buenos Aires Brownies Net wt. 1/4 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Junior Triple Trouble Chocolate Cookies Net wt. 6 ounces

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Graham Crackers 1 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Northern Corn Bread Net wt. 18 ounces

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Country Scone Net wt. 3 ounces

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Mary's Wild Oats Cranberry Almond Granola 1 lb

Zingerman's Bakehouse, Inc.

FDA Food Critical Dec 12, 2012

Organic Gelato Chocolate Peanut Butter, 5 liter, contained in plastic packaging, manufactured by Fresca Foods, CO.

Boulder Ice Cream

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Sweet Butter Teacake 1.25 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Townie Brownies Net wt. 1/4 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Black Magic Brownies Net wt. 1/4 lb

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Currant Scone Net wt. 3 ounces

Zingerman's Bakehouse, Inc.

FDA Food Moderate Dec 12, 2012

Zingerman's Bakehouse Summer Fling Coffeecake Net wt. 3 lbs

Zingerman's Bakehouse, Inc.

FDA Drug Moderate Dec 12, 2012

Fluorouracil Topical Cream USP, 5%, 40 g Tube, Rx only, Mfd. by: Taro Pharmaceutical Industries, Ltd. Haifa Bay, Israel 26110, Dist. by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532, NDC 51672-4118-6.

Taro Pharmaceuticals U.S.A., Inc.

FDA Drug Moderate Dec 12, 2012

Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL Genentech, South San Francisco, CA 94080, NDC#50242-0076-01

Genentech Inc

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP), 112 mcg., 100-count bottles, Rx only, NDC 0456-1330-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP), 137 mcg., 100-count bottles, Rx only, NDC 0456-1331-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.137 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP),125 mcg., 100-count bottles, Rx only, NDC 0456-1324-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP), 88 mcg., 100-count bottles, Rx only, NDC 0456-1329-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.050 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL Genentech, South San Francisco, CA 94080, NDC#50242-0074-01

Genentech Inc

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP), 300 mcg., 100-count bottles, Rx only, NDC 0456-1328-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.112 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St. Louis, MO, by Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.125 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

traMADOL Hydrochloride Tablets, USP 50 mg, 1000-count tablets per bottle, Manufactured by: Sun Pharmaceuticals Industries, Dadra 396 191, India; Distributed by: Caraco Pharmaceutical Laboratories, Ltd., 1150 Elijah McCoy Drive, Detroit, MI 48202; NDC 57664-377-18.

Caraco Pharmaceutical Laboratories, Ltd.

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.300 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Moderate Dec 12, 2012

Thyro-Tab 0.088 mg., packaged in 150,000-tablet bulk drums for repackaging, RX. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, IA.

Lloyd Inc. of Iowa

FDA Drug Low Dec 12, 2012

Novarel¿ (Chorionic Gonadotropin for injection, USP), 10,000 USP FOR INTRAMUSCULAR USE ONLY Rx Only NDC 55566-1501-0 Manufactured for : Ferring Pharmaceuticals Inc., Parsippany, NJ 07054 Manufactured by: DRAXIS Specialty Pharmaceuticals Inc., Quebec, Canada. NDC # 55566-1501-0 is assigned to the vial of NOVAREL and is displayed on the vial label. NDC # 55566-1501-1 is assigned to the unit of sale, which is a carton containing 1 vial of NOVAREL and 1 vial of diluent along with the

Ferring Pharmaceuticals Inc

FDA Devices Moderate Dec 12, 2012

Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the quantitative determination of iron in human serum and plasma on the Dimension Vista(R) System. Measurements of iron are used in the diagnosis and treatment of diseases such as iron deficiency anemia and other disorders of iron metabolism.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Dec 12, 2012

Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A REF 0702-001-000, Rx, Caution, consult accompanying documents Consult instructions for use, Max Vacuum; 21.0 in-Hg, 530 mm-Hg, The Neptune Waste Management System consists of a mobile rover unit used to suction and collect fluid waste, small debris and electrocautery smoke from a surgical site. Mobility allows the rover unit to be relocated to a waste disposal area where the rovers collection canisters can be emptied, via the docking station.

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Dec 12, 2012

24 Fr 8mm Soft Flow Ang W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Dec 12, 2012

Siemens Mobilette Mira, intended use as Mobile x-ray system.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 12, 2012

Stryker Orthopaedics TIBIAL OFFSET BUSHING TRIATHLON REVISION INSTRUMENTS REF 6543-2-600;NON-STERILE Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA A Subsidiary of Stryker Corp. Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France Made in USA The Offset Bushings are parts of the Triathlon TS system. They are used during trialing to assess the appropriate magnitude and orientation of offset between the Implant and the

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Dec 12, 2012

Stryker Orthopaedics FEMORAL OFFSET BUSHING TRITHION REVISION INSTRUMENTS REF 6543-1-600;NON-STERILE Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA A Subsidiary of Stryker Corp. Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France The Offset Bushings are parts of the Triathlon TS system. They are used during trialing to assess the appropriate magnitude and orientation of offset between the Implant and the intramedullary S

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Dec 12, 2012

OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is indicated for the incision, excision, ablation, vaporization and coagulation of body soft tissues including intra-oral tissues. It is indicated in the medical specialties of general and plastic surgery, oral/maxillofacial surgery, dentistry, dermatology, gynecology, otorhinolaryngology, gastroenterology, neurosurgery, urology, and pulmonology, and can be used in open surgical procedures as well as e

OmniGuide, Inc.

FDA Devices Moderate Dec 12, 2012

24 Fr 8mm Sft Flow Straight Wir The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Dec 12, 2012

Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended for use by healthcare professionals to monitor vital signs for patients undergoing MRI procedures. The Patient Monitoring System also provides signals for synchronization to the MR scanner.

Invivo Corporation

FDA Devices Moderate Dec 12, 2012

Philips Digital Diagnost Software Version R2.0.2 Product Usage: This system is used for making X-ray exposures for diagnostics

Philips Healthcare Inc.

FDA Devices Critical Dec 12, 2012

The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for treatment of hypoxic-ischemic encephalopathy (HIE) in infants. A cooling water cap is placed on the infant's head and the body is warmed using radiant warmers. The Cool-Cap provides 72 hours of monitored cooling. The device is labeled in parts: "***OLYMPIC COOL-CAP Cooling Unit***Natus Medical Incorporated 5900 First Avenue South ***Made in USA***Control Unit Model No. 60010**

Natus Medical Incorporated

FDA Devices Moderate Dec 12, 2012

24 Fr 8mm Sft Flow Str Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery. These devices are indicated for up to 6 hours of use.

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Dec 12, 2012

Sekisui Diagnostics, Spectrolyse PAI-1 In-Vitro Diagnostic Use for the quantitative determination of Plasminogen Activator Inhibitor Type 1 in human plasma. Catalog # 101201. Spectrolyse PAI-1 is intended for the quantitative determination of Plasminogen Activator Inhibitor Type-1 (PAI-1) activity in human plasma. The test is for in vitro diagnostic use.

Sekisui Diagnostics 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.