PlainRecalls

2013 Recalls

6,215 recalls · Page 123 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 6 critical, 34 moderate, and 10 lower-severity recalls. The page references 32 distinct recalling firms operating in 7 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), CPSC (9), FDA Food (8), 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 Food Critical Jan 16, 2013

Kinnikinnick Pie Crust Gluten Free (frozen) weight 290 g/ 10 oz Qty/Pkg: 2, UPC 620133006229, Kinnikinnick Foods 10940 120 Street, Edmonton, AB Canad…

United National Foods (Unfi)

FDA Food Critical Jan 16, 2013

Alaskan Wild Smoked Sockeye Salmon in vacuum packed plastic package, labeled in part: "MICHAEL'S WILD SOCKEYE SMOKED SALMON***IN…

Michael's Seafood Inc. DBA Michael's Gourmet & Delicacies

FDA Devices Low Jan 16, 2013

Immunoradiometric assay. Device is an immunoradiometric assay designed for the quantitative measurement of thyroid stimulating hormone (thyrotropi…

Siemens Healthcare Diagnostics

FDA Devices Moderate Jan 16, 2013

PT113950 PT HYBRID Glenoid Post Regenerex porous titanium construct Sterile R Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Biomet, Inc.

FDA Devices Moderate Jan 16, 2013

(l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring Arm Circlip is part of the S…

Stryker Communications, Inc.

FDA Devices Moderate Jan 16, 2013

CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support t…

Maquet Cardiovascular, LLC

FDA Devices Moderate Jan 16, 2013

Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured by Philips Medical Systems, Seattle, WA 98121 USA; and Laerdal branded FR…

Philips Medical Systems North America Co. Phillips

FDA Devices Moderate Jan 16, 2013

Merit Medical's Custom Procedural Tray or Kits K12T-03162B & K12T-02641F.Custom Procedural Tray or Kits is a combination of legally marketed…

Merit Medical Systems, Inc.

FDA Devices Moderate Jan 16, 2013

Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #2.5 and Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem #3.5, Howmedica Osteonics Corp…

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Jan 16, 2013

Sterile Rigid Tip Suction Wand The Suction Wands are indicated for use to remove excess fluid from the surgical field.

California Medical Laboratories Inc

FDA Devices Low Jan 16, 2013

Immunoradiometric assay.

Siemens Healthcare Diagnostics

FDA Devices Moderate Jan 16, 2013

UltraFill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 5cc Product Code: RT53005 Donated Human Tissue All…

Surgical Tissue Network, Inc.

FDA Devices Moderate Jan 16, 2013

AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor…

Zoll Circulation, Inc.

FDA Devices Low Jan 16, 2013

Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry Catalog Number:1360 Chek-Stix¿ Positive and Negative Control Strips fo…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jan 16, 2013

Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R) Phenobarbital Assay (4D019UL). Homogeneous enzyme immunoassay intended for use in …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 16, 2013

UltraFill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 10cc Product Code: RT53010 Donated Human Tissue A…

Surgical Tissue Network, Inc.

FDA Devices Low Jan 16, 2013

Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364M Chek-Stix¿ Positive and Negative Control Strips for Urine Chemistry: Whe…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jan 16, 2013

Ultrafill DBM labeled in part: TISSUENET Sterilized by T10^6 Description: UltraFill DBM Size: 1cc Product Code: RT53001 Donated Human Tissue Allograf…

Surgical Tissue Network, Inc.

FDA Devices Low Jan 16, 2013

Siemens Chek-Stix Positive and Negative Control Strips for Urine Chemistry (Distributed OUS Only) Catalog Number: 1360L Chek-Stix¿ Positive and …

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jan 16, 2013

The TM Ardis Interbody System Inserter Stainless Steel, Rubber, Silicone Non Sterile Rx only. The TM Ardis Inserter is intended for delivery of th…

Zimmer, Inc.

FDA Devices Moderate Jan 16, 2013

Siemens Chek-Stix Combo Pak (Distributed OUS only) Catalog Number: 1364N Chek-Stix¿ Positive and Negative Control Strips for Urine Chemistry: W…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jan 16, 2013

ABX PENTRA ML, Software Versions: V8.0.x and Below; V.9.0.1 and V9.0.2

Horiba Instruments, Inc dba Horiba Medical

FDA Devices Moderate Jan 16, 2013

Rigid Tip Suction Wand Non sterile bulk devices (S112468N, S120196N, and S120197N) were sold to Terumo UK to be included in a kit under Terumo as ma…

California Medical Laboratories Inc

FDA Devices Low Jan 16, 2013

Siemens Chek-Stix Combo Pak Catalog Number: 1364 Chek-Stix¿ Positive and Negative Control Strips for Urine Chemistry: When used with Siemens rea…

Siemens Healthcare Diagnostics Inc

FDA Devices Low Jan 16, 2013

Siemens Emit(R) tox(TM) Serum Calibrators, catalog number 7B019UL The Emit(R) tox(TM) Serum Calibrators are intended for use with the Emit(R) tox(…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Jan 16, 2013

FlowGate Balloon Guide Catheter; Manufactured by Concentric Medical, Mountain View, CA. FlowGate&quot…

Concentric Medical Inc

FDA Devices Low Jan 16, 2013

Siemens Chek-Stix Combo Pak (Distributed OUS) Catalog Number: 1364E Chek-Stix¿ Positive and Negative Control Strips for Urine Chemistry: When us…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jan 16, 2013

STERRAD NX Cassettes, P/N 10133. The STERRAD NX sterilizations systems are low-temperature general purpose sterilizers used to sterilize heat and …

Advanced Sterilization Products

FDA Devices Moderate Jan 16, 2013

Laparoscope, general; plastic surgery Used for general, abdominal, gynecological and thoracic minimally invasive surgical procedures to establish …

Applied Medical Resources Corp

FDA Devices Low Jan 16, 2013

Immunoradiometric assay. Device is an immunoradiometric assay designed for the quantitative measurement of thyroid stimulating hormone (thyrotropi…

Siemens Healthcare Diagnostics

FDA Devices Moderate Jan 16, 2013

Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model number M5066A, M5067A, and M5068A Automated External Defibrillator Manufact…

Philips Medical Systems North America Co. Phillips

FDA Devices Low Jan 16, 2013

Siemens CLINITEK Atlas Positive and Negative Control Strips for Urine Chemistry Catalog Number: 5019 When used with the CLINITEK ATLAS¿ Automate…

Siemens Healthcare Diagnostics Inc

CPSC Moderate Jan 16, 2013

Powertec Recalls Weight Workbenches Due to Injury Hazard

CPSC Moderate Jan 16, 2013

Target Recalls Hand-Held Air Misters Due to Injury Hazard

CPSC Moderate Jan 15, 2013

Bugaboo Recalls Strollers Due to Fall and Choking Hazards

Bugaboo International B.V., of Amsterdam, The Netherlands

CPSC Moderate Jan 15, 2013

KTM North America Recalls Enduro Motorcycles Due to Fuel Leak, Fire and Crash Hazard

KTM-Sportmotorcycle AG, of Mattighofen, Austria

CPSC Moderate Jan 15, 2013

Target Recalls Children's Two-Piece Pajama Sets Due to Violation of Federal Flammability Standard

Makalot Garments Co. Ltd., of Taiwan

CPSC Moderate Jan 15, 2013

Target Recalls Circo Girls Fleece Pajamas Due to Violation of Federal Flammability Standard

NHTSA Critical Jan 14, 2013

CHEVROLET,GMC 2013: ELECTRICAL SYSTEM:IGNITION

CHEVROLET,GMC

CPSC Moderate Jan 10, 2013

BRP Recalls Can-Am Side-By-Side Vehicles Due to Loss of Steering Control Hazard

BRP Mexico S.A. de C.V., of Juarez, Chihuahua, Mexico

CPSC Moderate Jan 10, 2013

High-Pressure Scuba Diving Air Hoses Recalled by A-Plus Marine Due to Drowning Hazard

CPSC Moderate Jan 10, 2013

John Deere Recalls Gator Utility Vehicles Due to Fire Hazard

Deere & Company of Moline, Ill.

FDA Food Moderate Jan 9, 2013

Cocoa~Latte Hot Drink Maker; an electric hot drink mixer and dispenser with a 32 fl.oz. heating and mixing jar, twist and lock lid, "perfect temperat…

Focus Products Group Llc

FDA Food Critical Jan 9, 2013

La Madeleine Potato Soup, 5 lb clear Cryovac pouches, 4 pouches per case.

Gourmet Cuisine, Inc.

FDA Food Moderate Jan 9, 2013

Sanh Yuan Preserved Plum Candy (Sweet and Sour Prune), 5 oz (142g)

Cho Fuku Group (usa) Inc

FDA Food Critical Jan 9, 2013

Fresh Express brand, Fresh Spinach, 9 oz.

Fresh Express Incorporated

FDA Food Moderate Jan 9, 2013

Nature's Plus GLUTEN Free SPIRU-TEIN HIGH PROTEIN ENERGY MEAL, S'mores (Flavor), 1.2 OZ. (34g) Packet, Display Box Product No. 95903, Individual Pack…

Natural Organics

FDA Food Moderate Jan 9, 2013

Hemp Plus Granola. The product is packaged in a 25 lb. container. The UPC is 0 58449 88001 1. The product is labeled in parts: "***HempPlus Gran…

Nature'S Path Foods Inc

FDA Drug Critical Jan 9, 2013

Methylprednisolone Acetate (PF) 40 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

Glycerin 100% PF, 1mL, 2 mL, and 5 mL vials, manufactured by New England Compounding Center, Framingham, MA

New England Compounding Center

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