PlainRecalls

2013 Recalls

6,215 recalls · Page 124 of 125

2013 Recall Year Insight

Federal agencies issued 6,215 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 7.40% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.0 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 125 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 2013.

On this page of 50 records, severity classification shows 8 critical, 40 moderate, and 2 lower-severity recalls. The page references 26 distinct recalling firms operating in 7 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Drug (23), FDA Devices (19), CPSC (5), 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 2013 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 Drug Critical Jan 9, 2013

Methylprednisolone Acetate 40 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingh…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Isovue 200 mg/mL PF and 300 mg/mL PF, Vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Omnipaque 240mg/mL PF, 300mg/mL PF, in 3 mL, 5 mL, and 10 mL, vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Saline 10% and 3%, in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Triamcinolone 10 mg/mL P, 40mg/mL P, 40mg/mL PF and 80 mg/mL PF in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Lidocaine 1% PF, 2% PF, and 4% PF, in 1 mL, 2 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Epinephrine Injection USP, 1 mL, USP 1:1000 (1 mg/mL), SQ/IM, Hospira, Inc., Lake Forest, IL --- NDC 0409-7241-01

Hospira Inc.

FDA Drug Moderate Jan 9, 2013

Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6 mg/mL P Injection, manufactured by New England Compounding Center, Frami…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Betamethasone Sodium Phosphate 6 mg/mL P Injection, Betamethasone Sodium Phosphate 6 mg/mL PF Injection, Betamethasone Sodium Phosphate 8 mg/mL PF…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Bupivacaine 0.25% PF, Bupivacaine 0.5% PF, and Bupivacaine 0.75% PF, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Critical Jan 9, 2013

Methylprednisolone Acetate (PF) 80 mg/ml Injection, supplied in 1 mL, 2 mL and 5 mL vials, manufactured by New England Compounding Center, Framingham…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Clonidine 100 mcg/mL PF, 1mL and 2 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Lidocaine/Dextrose 5%/7.5% PF, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Drug Critical Jan 9, 2013

Methylprednisolone Acetate 80 mg/mL Injection, Preserved, supplied in 5 mL and 10 mL vials, manufactured by New England Compounding Center, Framingh…

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Dexamethasone Sodium Phosphate 4 mg/mL vials PF, 6 mg/mL PF vials, and 8 mg/mL PF vials, manufactured by New England Compounding Center, Framingham, …

New England Compounding Center

FDA Drug Moderate Jan 9, 2013

Synthroid (Levothyroxine Sodium) tablets, 150 mcg (0.15 mg), 90 tablets per bottle, Rx Only, NDC 0074-7069-90; ABBOTT LABORATORIES NORTH CHICAGO, IL …

Abbott Laboratories

FDA Drug Moderate Jan 9, 2013

Hyaluronidase 150 u/ml PF, 1 mL, 5 mL, and 10 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

FDA Devices Moderate Jan 9, 2013

Plum A+ Hyperbaric Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; list number 11005 Product Usage: The Plum A+ Hyperbaric Infus…

Hospira Inc.

FDA Devices Moderate Jan 9, 2013

Abbott m2000sp Instrument; an automated fluid handling system for performing sample preparation for nucleic acid testing; Abbott Molecular Inc., Des …

Abbott Molecular

FDA Devices Moderate Jan 9, 2013

Plum A+3 Triple Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following configurations: a) list 12348 -…

Hospira Inc.

FDA Devices Moderate Jan 9, 2013

DPM Central Station Mindray DS USA, Inc. 800 MacArthur Boulevard, Mahwah, NJ 07430 The Central Monitoring Station (CMS) network transfers informa…

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

FDA Devices Moderate Jan 9, 2013

Space Pump Pole Clamps for the Infusomat Space Pump, model number 8713130. The Pole Clamp is an accessory to Space Pumps designed to support 1 to …

B. Braun Medical, Inc.

FDA Devices Moderate Jan 9, 2013

Plum A+ Single Channel Infusion Pumps; Hospira, Inc., Lake Forest, IL 60045; the pumps were sold under the following configurations: a) list 11971; b…

Hospira Inc.

FDA Devices Moderate Jan 9, 2013

Medical Surgical Bed, Model 3005S3EX Medical Surgical Bed The S3" MedSurg Bed, Model 3005 is intended to support and transport patients within the…

Stryker Medical Division of Stryker Corporation

FDA Devices Low Jan 9, 2013

Fast-Cath Transseptal Guiding Introducer, 90, 8F, REF 406586, Length 60 cm, Sterile EO, Rx only, St. Jude Medical, 14901 DeVeau Place, Minnetonka, MN…

St Jude Medical Inc

FDA Devices Moderate Jan 9, 2013

Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Kehler Strabe 31 Baden-Wuerttemberg 76437 Rastatt,Germany Used to support the lower e…

Maquet Inc.

FDA Devices Low Jan 9, 2013

Analyzing system consists of a small and portable analyzer and plastic microcuvettes. The microcuvette contains reagents deposited on its inner walls…

HemoCue AB

FDA Devices Moderate Jan 9, 2013

Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting situations. It can be used with …

Hill-Rom, Inc.

FDA Devices Moderate Jan 9, 2013

AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses

Cooper Vision Caribbean Corp.

FDA Devices Moderate Jan 9, 2013

Companion External Battery, Part Number: 293001-001 The Companion External Battery is a component of the Companion 2 Driver System and the Compani…

SynCardia Systems Inc.

FDA Devices Moderate Jan 9, 2013

ABX PENTRA AST CP, Part Number: A11A01629. The ABX Pentra AST CP reagent is a diagnostic reagent for quantitative in vitro determination of Aspart…

Horiba Instruments, Inc dba Horiba Medical

FDA Devices Moderate Jan 9, 2013

Medical Surgical Bed, Model 3002SEX Medical Surgical Bed The S3" MedSurg Bed, is intended to support and transport patients within the Med/Surg an…

Stryker Medical Division of Stryker Corporation

FDA Devices Moderate Jan 9, 2013

PENTRA C200, Part Number: A11A01629. The Pentra C200 system is a fully automated chemistry analyzer using colorimetry, turbidmetry and potentiomet…

Horiba Instruments, Inc dba Horiba Medical

FDA Devices Critical Jan 9, 2013

Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing circuit, 1.8m or 6 feet in length. Oxygen therapy delivery system for…

Fisher & Paykel Healthcare, Ltd.

FDA Devices Moderate Jan 9, 2013

Medtronic Intersept Custom Tubing Pack with or without coating ( Carmeda BioActive Surfact, Carmeda BioActive Surfact and Trillium Biosurface,or Bala…

Medtronic Inc. Cardiac Rhythm Disease Management

CPSC Moderate Jan 9, 2013

Columbia Sportswear Reannounces Its Recall of Batteries Sold With Jackets Due To Fire Hazard

CPSC Moderate Jan 9, 2013

Polaris Recalls Ranger Recreational Off-Highway Vehicles Due to Loss of Control and Crash Hazard

Polaris Industries Inc., of Medina, Minn.

CPSC Moderate Jan 8, 2013

Fisher-Price Recalls to Inspect Rock 'N Play Infant Sleepers Due to Risk of Exposure to Mold

CPSC Moderate Jan 8, 2013

PLATINUM Neon Sign Power Supply Transformers Made by HEICO lighting Recalled Due To Fire Hazard

HEICO lighting, a division of EMD Technologies, of Montreal, Quebec, Canada

CPSC Moderate Jan 4, 2013

Goodman Company Recalls Amana Heating and Cooling Units Due to Fire Hazard

Goodman Company L.P., of Houston, Texas

FDA Food Critical Jan 2, 2013

CMC Pumpkin Coffee Cake 16 oz UPC: 041735225726 Price Chopper/Box

Golub Corp

FDA Food Critical Jan 2, 2013

Spence & Co New York-Style Nova Lox 4oz , refrigerated Spence & Co Smoked Salmon Trimmings, 2lb bulk (bag)

Spence & Co., Ltd.

FDA Food Critical Jan 2, 2013

Taylor Farms Hearts of Romaine Lettuce, All Natural, Fresh Hand Selected, Triple Washed and Ready to Enjoy. 10 oz. bags. Taylor Farms, Salinas, CA. …

Taylor Farms Retail, Inc.

FDA Drug Moderate Jan 2, 2013

Cymevene 500 mg Powder for Infusion, (ganciclovir), 50 mg/mL ganciclovir (reconstructed), Rx only, 10 mL vials, Roche Products Limited, Welwyn Garden…

F. Hoffmann-LaRoche Ltd.

FDA Drug Moderate Jan 2, 2013

Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc…

Lloyd Inc. of Iowa

FDA Drug Moderate Jan 2, 2013

Levothroid (levothyroxine sodium tablets, USP), 50 mcg., 100-count bottles, Rx only, NDC 0456-1321-01, Manufactured for Forest Pharmaceuticals, Inc…

Lloyd Inc. of Iowa

FDA Drug Moderate Jan 2, 2013

Levothyroxine Sodium Tablets, USP, 175 mcg in 90 ct bottles, Manufactured by Patheon Puerto Rico Inc., for Alara Pharmaceutical Corp, San Juan, PR

Alara Pharmaceutical Co

FDA Drug Moderate Jan 2, 2013

Thyro-Tab 0.075 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 Jan 2, 2013

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 Devices Critical Jan 2, 2013

Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Catalog Number: OX-M-AEGNGVNTG Usage: Regulator reduces pressure in oxygen-containin…

Praxair Inc.

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2013 with 2012 →

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 2013