PlainRecalls

2012 Recalls

4,173 recalls · Page 71 of 84

2012 Recall Year Insight

Federal agencies issued 4,173 product recalls indexed by PlainRecalls in calendar year 2012. That represents about 4.10% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 11.4 recalls per day across the FDA, CPSC, 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 4 critical, 36 moderate, and 10 lower-severity recalls. The page references 22 distinct recalling firms operating in 5 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (35), FDA Drug (11), FDA Food (2), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Low Jul 11, 2012

Northern Catch Harvest of the Sea Fancy Whole Oysters and SeaNet Fancy Whole Oysters; Net Wt. 8 oz (227g) cans, 12 cans per carton; Distributed by Al…

Aldi Inc

FDA Food Critical Jul 11, 2012

MUFFINS PLAIN (MEXICAN SWEET BREAD) IMPORTED BY EL CHARRO MEXICANTOWN BAKERY DETROIT MI 48210 4.0oz 21-MAY-12

Mexicantown Wholesale

FDA Drug Low Jul 11, 2012

Balnetar Therapeutic Tar Bath, Coal Tar USP 2.5% (from Coal Tar USP Solution, 7%), 7.5 oz bottle, Distributed by Ranbaxy, Jacksonville, FL 32257, NDC…

Ranbaxy Inc.

FDA Drug Low Jul 11, 2012

Loxapine Capsules USP, 5mg, 100 count bottle, Rx only Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 00591-0369-01.

Watson Laboratories Inc

FDA Drug Low Jul 11, 2012

Loxapine Capsules USP, 50mg, 100 count bottle, Rx only Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 0591-0372-01

Watson Laboratories Inc

FDA Drug Moderate Jul 11, 2012

Metoprolol Tartrate Tablets USP 50 mg, 1000 count bottle, Rx only, Manufactured in india By: Emcure Pharmaceuticals LTD. Hinjwadi, Pune, India, Manuf…

Teva Pharmaceuticals USA, Inc.

FDA Drug Low Jul 11, 2012

Loxapine Capsules USP, 10mg, 100 count bottle, Rx only, Manufactured By: Watson Laboratories Inc., Corona, CA 92880 Rx only. NDC # 0591-0370-01

Watson Laboratories Inc

FDA Drug Low Jul 11, 2012

Imodium Multi-Symptom Relief Caplets, Loperamide HCl 2 mg/Simethicone 125 mg, 18 count blister pack cartons, McNeil Consumer Healthcare, Div of McNei…

Mcneil Consumer Healthcare, Div Of Mcneil-ppc, Inc.

FDA Drug Low Jul 11, 2012

Super Colon Cleanse, stimulant laxative, 140 mg of Senna per capsule, 25 doses, 100 capsules, Manufactured by: healthPLUS Inc. Chino, CA 91710 USA.

Health Plus Incorporated

FDA Drug Moderate Jul 11, 2012

Eloxatin (OXALIplatin injection) 5 mg/mL Injection, 50 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 08807, NDC 0024-0590-10

sanofi-aventis US, Inc.

FDA Drug Low Jul 11, 2012

Loxapine Capsules USP, 25mg, 100 count bottle, Rx only, Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 0591-0371-01

Watson Laboratories Inc

FDA Drug Moderate Jul 11, 2012

Eloxatin (OXALIplatin injection) 5 mg/mL injection, 100 mg, Rx only, Mfd. for: sanofi aventis US LLC Bridgewater, NJ 08807, NDC 0024-0591-20

sanofi-aventis US, Inc.

FDA Drug Low Jul 11, 2012

Loxitane Capsules, Loxapine Succinate Capsules, 10mg base, 100 count bottle, Rx only, Watson Laboratories Inc., Corona, CA 92880 NDC # 52544-495-…

Watson Laboratories Inc

FDA Devices Moderate Jul 11, 2012

Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and da…

Philips Healthcare Inc.

FDA Devices Low Jul 11, 2012

Single Shot Epidural Trays, Sterile, Integra Pain Management, West Valley City, Utah 84119, each kit contains sterile instruments, drugs and other me…

Integra LifeSciences Corp. d.b.a. Integra Pain Management

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 1 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 283904611. The Confidence Sid…

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 3 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were packaged …

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 9 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ1 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Fo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 5 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector; an Rx device for single patient use; 30 connectors per box; CareFusion, …

Carefusion 2200 Inc

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/4M Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foa…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/2M Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foa…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/1M Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foa…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 10 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were packag…

DePuy Orthopaedics, Inc.

FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an Rx device for single patient use; CareFusion, 22745 Savi Ranch Parkw…

Carefusion 2200 Inc

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ4 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Fo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one. The Quick shield Complete Plus is intended to be used only with Vacue…

Greiner Bio-One North America, Inc.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 6 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Revision Instruments assist in the removal of an occipital cervical screw during…

Aesculap Implant Systems LLC

FDA Devices Moderate Jul 11, 2012

Victory 9 with Power Seat (SC609PS) Motorized wheelchair with elevating seat.

Pride Mobility Products Corp

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 7 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Critical Jul 11, 2012

AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Heated; an Rx device for single patient use; CareFusion, 22745 Savi Ranch Parkway, …

Carefusion 2200 Inc

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ3 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Fo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

TDX SP Power Wheelchair, TDX SR Power Wheelchair, TDX SI Power Wheelchair. Model Number(s): TDXSI, TDXSI-2, TDXSI-2-S, TDXSI-CG, TDXSI-HD, TDXSI-HD-S…

Invacare Corporation

FDA Devices Moderate Jul 11, 2012

Depuy Spine Side Fire Needles 13G X 6IN, part of the Confidence Spinal Cement System Product Code 283904613. The Confidence Side Fire Needle is …

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 4 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

Depuy Spine Side Fire Needles 11G X 4IN, part of the Confidence Spinal Cement System Product Code: 283904411. The Confidence Side Fire Needle is …

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ5 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Fo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

Depuy Spine Side Fire Needles 13G X 4IN Side-Fire Needle, part of the Confidence Spinal Cement System Product Code 283904413. The Confidence Side…

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/SZ2 Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Fo…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 8 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

ULTIMA*LX STM,POL 10/12TAP/3M Packaging: The product was packaged within inner and outer PETG blister trays and sealed with coated Tyvek lids. Foa…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

AirLife¿ MiniSpacer¿ MDI Dispenser Adapter. Dual-Spray MiniSpacer¿ Metered Dose Inhaler (MDI) Dispenser/Adapter with 15 mm connections. The 15 mm…

Thayer Medical Corporation

FDA Devices Moderate Jul 11, 2012

Microbiologics 217 Osseo Avenue North, St. Cloud, MN 56303, Gram Stain Control Slides, SLO3-10, ATCC Licensed Derivative, MediMart Europe, 11 rue Em…

Microbiologics Inc

FDA Devices Moderate Jul 11, 2012

LUSTER HIP SZ 2 Packaging: The product was packaged within inner and outer blister trays, sealed with coated Tyvek lidding. The stems were package…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 11, 2012

PathFinder NXT Pivoting Percutaneous Rod Holder This device is an instrument used during orthopedic surgery. The intended use of the pivoting perc…

Zimmer, Inc.

CPSC Moderate Jul 11, 2012

Nikon Recalls Rechargeable Battery Packs Sold with Digital SLR Cameras Due to Burn Hazard

Nikon Inc., of Melville, N.Y.

CPSC Moderate Jul 11, 2012

Troxel Recalls Flexible Flyer Swing Sets Due to Fall Hazard

The Troxel Company, of Moscow, Tenn.

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 - consumer product and vehicle recall feeds for 2012

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2012 across the FDA, CPSC 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 August 2026.