PlainRecalls

2013 Recall Year Insight

Federal agencies issued 6,262 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 6.00% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.2 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 126 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 9 critical, 36 moderate, and 5 lower-severity recalls. The page references 30 distinct recalling firms operating in 6 distinct product categories, with 44 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (18), FDA Devices (14), FDA Drug (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 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, 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 Aug 28, 2013

00595001201 Femur CR-FLEX PCT FEM B-L Rx, Sterile; 00595001202 Femur CR-FLEX PCT FEM B-R Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

Product Name: nanoPOINT Injector System, item number 37-0000-08. Intended to fold and insert a STAAR Surgical Collamer¿ nanoFLEX or Afinity IOLs, through surgical procedure in a human eye.

Medicel Ag

FDA Devices Moderate Aug 28, 2013

00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10, Rx, Sterile; 00597604112 Articular Surface AC ART SURF 56/STRIPED GRN 12, Rx, Sterile; 00597604114 Articular Surface AC ART SURF 56/STRIPED GRN 14, Rx, Sterile; 00597604117 Articular Surface AC ART SURF 56/STRIPED GRN 17, Rx, Sterile; 00597604120 Articular Surface AC ART SURF 56/STRIPED GRN 20, Rx, Sterile; 00597604123 Articular Surface AC ART SURF 56/STRIPED GRN 23, Rx, Sterile; Used in total knee arthroplasty and in

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

PleuraGuide Disposable Chest Tube Kit; Product codes: 17100, 17150, and 17200. Indicated to assist with the insertion of thoracic catheters.

Atrium Medical Corporation

FDA Devices Moderate Aug 28, 2013

90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17, Rx, Sterile; 90595204120 Articular Surface XLPE CR ART SURF AE56/STGRN 20, Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

Edwards Lifesciences Suction Wand Model S099B, packaged in Sorin Group Heart/Lung Perfusion Packs.

Sorin Group USA, Inc.

FDA Devices Moderate Aug 28, 2013

65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx, Sterile; 65597201132 Femur CR POR FEM SURF HDN HATCP AMR Rx, Sterile; 65597201231 Femur CR POR FEM SURF HDN HATCP BML Rx, Sterile; 65597201232 Femur CR POR FEM SURF HDN HATCP BMR Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

Stryker Visum 300 Ceiling-mounted Exam Light.

Stryker Communications

FDA Devices Moderate Aug 28, 2013

00597001131 Femur CR PRC SURF HDN FEM CO-NID AML, Rx, Sterile; 00597001132 Femur CR PRC SURF HDN FEM CO-NID AMR, Rx, Sterile; 00597001231 Femur CR PRC SURF HDN FEM CO-NID BML, Rx, Sterile; 00597001232 Femur CR PRC SURF HDN FEM CO-NID BMR, Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

The Discovery NM/CT 570c CT Standalone Scan The Discovery NM/CT 570c hybrid system is a combination of a cardiac dedicated nuclear imaging subsystem and LightSpeed GE CT subsystem. This system is intended for cardiac Nuclear Medicine (NM) diagnostic imaging applications, head and body CT diagnostic imaging applications, as well as attenuation correction and anatomical localization. The Discovery product is a SPECT-CT system. It consists of two back-to-back gantries, the NM Gantry, carrying s

GE Healthcare, LLC

FDA Devices Moderate Aug 28, 2013

90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17, Rx, Sterile; 90595203120 Articular Surface XLPE CR ART SURF AE34/STYEL 20, Rx, Sterile; Used in total knee arthroplasty and indicated for patients with severe pain.

Zimmer, Inc.

FDA Devices Moderate Aug 28, 2013

Boston Scientific, ENERGEN DR ICD, Model E143. The device is an Implantable Cardioverter Defibrillator.

Boston Scientific CRM Corp

FDA Devices Moderate Aug 28, 2013

Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure, Latex Free Sterile EO Rx, 1/4" X 4 ", 6 mm X100 mm, (2 Cards/pouch, 1,000 Pouches/box); Distributed in Europe: " Product Number: 39-0058: Medicare Reinforced Wound Closure Strips 1/4" X 4 ", Sterile, Box 1000 pouches 5 strips /pouch, Pouch , 5 strips 6 mm X100 mm Sterile EO Product Number: 40-2893: Wound Closure Strips , Sterile (1,000pouches/box) Rx; Pouch Label: Wound Closure Strips 6 mm X100 mm, 1/4" X 4 ",

Aspen Surgical Products, Inc.

FDA Devices Low Aug 28, 2013

ConvaTec Flexi-Seal SIGNAL Fecal Management System, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.

Convatec Inc.

CPSC No agency class Aug 28, 2013

Baby Jogger Recalls Car Seat Adaptors for Strollers Due to Fall Hazard

CPSC No agency class Aug 28, 2013

Vitamix Recalls 64-Ounce Low Profile Blender Container Due to Laceration Hazard

Vita-Mix Corporation of Cleveland, Ohio

NHTSA No agency class Aug 28, 2013

LEXUS,TOYOTA 2006-2011: SUSPENSION:REAR

LEXUS,TOYOTA

NHTSA No agency class Aug 27, 2013

HONDA 2013: ENGINE

HONDA

NHTSA No agency class Aug 23, 2013

FORD 2012: ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:MANIFOLD/HEADER/MUFFLER/TAIL PIPE

FORD

FDA Food Moderate Aug 21, 2013

individual 2 oz chocolate macaroons packaged in plastic wrapper labeled as " Jennies DUTCH CHOCOLATE MACAROON, 2 oz. Red Mill Farms, Inc., Brooklyn, NY".

Red Mill Farms

FDA Food Low Aug 21, 2013

Square Mile Spur & Vine Hopped Apple Cider is hopped hard cider is in liquid form and is an alcoholic beverage. It is packaged in 22 fl oz glass bottles shipped in a corrugated master carton that contains 12 bottles. Individual bottle is sold at retail stores. UPC codes case: 7-02770-04912-0 UPC Bottle: 7-02770-24910-0 PDCN code: CAB12

Craft Brewers Alliance Inc.

FDA Food Moderate Aug 21, 2013

Shoreline Fruit Dark Chocolate Covered Dried Balaton Cherries 25lbs

Shoreline Fruit Inc

FDA Food Low Aug 21, 2013

Square Mile Original Hard Apple Cider is hard cider is in liquid form and is an alcoholic beverage. It is packaged in 22 fl oz glass bottles shipped in a corrugated master carton that contains 12 bottles. Individual bottle is sold at retail stores. UPC codes case: 7-02770-04812-0; UPC Bottle: 7-02770-24810-0; PDCN code: CAA12.

Craft Brewers Alliance Inc.

FDA Food Critical Aug 21, 2013

RYBACKA WIES brand HERRING FILLETS IN OIL (MATJES SLEDZ W OLEJU), Net Wt. 17.6 oz. (500g), UPC 0 21143 24122 8, Distributed By Gold Star, Inc., Brooklyn, NY 11231 --- The product is vacuum packed in a sealed plastic package.

Gold Star Smoked Fish Corp.

FDA Food Critical Aug 21, 2013

Crave Brothers Farmstead Classics Les Freres Semi-Soft French Style Cheese, LF225. 2.5 lb wheel packaged in cheese paper. Two 2.5 lbs wheels in a case.

Crave Brothers Farmstead Cheese, LLC

FDA Food Critical Aug 21, 2013

Chocolate malted milk balls packaged in 6 lbs. bags and each case contains 3 x 6 lbs. bags; BEST BY 04/17/14; BRCH CHOC

Ferrara Candy Company

FDA Food Moderate Aug 21, 2013

"***Gasco Golden Egg Yellow Shade Liquid***" 32 oz plastic bottles & 15 gallon drums

Gasco Industrial

FDA Food Critical Aug 21, 2013

Crave Brothers Farmstead Classics Petit Frere Soft Ripened Cheese, PF88. Net Wt. 8 oz. (227g). Packaged in cheese paper and sold inside a wooden box. Eight 8 oz wheels per case.

Crave Brothers Farmstead Cheese, LLC

FDA Food Moderate Aug 21, 2013

Cherry Bay Orchards Dark Chocolate Covered Dried Balaton Cherries 4lb, 8oz, and 16oz containers

Shoreline Fruit Inc

FDA Food Moderate Aug 21, 2013

Bulk tablet label: Keytabs W.O. Glandulars (pink)

Ancient Formulas Inc

FDA Food Critical Aug 21, 2013

FOSFOREL brand Herring Fillet in Oil 400 gram (14 oz.) in plastic packaging containers; refrigerated

Zip International Group LLC.

FDA Food Moderate Aug 21, 2013

Tortillas Lupita White Corn Tortillas, Manufactured by Tortilleria Lupita, 235 SW 25th St, Oklahoma City, OK 73109

Tortilleria Lupita, Inc.

FDA Food Moderate Aug 21, 2013

IMAGIC Vegetarian Burger Mix, VB 100, textured vegetable protein, contains soy and wheat, packaged in 25-lb/bulk cartons. CHS Inc., Hutchinson, KS.

C H S Inc

FDA Food Critical Aug 21, 2013

Crave Brothers Farmstead Classics Petit Frere with Truffles Cheese, PF88T. Net Wt. 8 oz. (227g). Packaged in cheese paper and sold inside a wooden box. Eight 8 oz. wheels per case.

Crave Brothers Farmstead Cheese, LLC

FDA Food Low Aug 21, 2013

Asian Taste Sun Flower Seeds, 40pk/carton, Net Wt: 8-oz. (227g), Item #1641819, UPC 6 919037 022708.

Walong Marketing, Inc.

FDA Food Moderate Aug 21, 2013

KEYTABS (Without Iron, Copper or Glandulars), packaged in 180-tablet bottles, a product of The Key Company, St. Louis, MO.

Ancient Formulas Inc

FDA Food Moderate Aug 21, 2013

Spartan Fresh Dark Chocolate Covered Dried Cherries 8oz

Shoreline Fruit Inc

FDA Drug Moderate Aug 21, 2013

HCG Chorionic Gonadotropin, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Vancomycin Ophthalmic PF, compounded by Pallimed Solutions Pharmacy, Wobrun, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Propofol Injectable Emulsion, 1%, 1 g/100 mL (10 mg/mL), 100 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-24; Propofol Injectable Emulsion, 500 mg/50 mL, 50 mL, Single patient infusion vial, RX only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-33

Hospira Inc.

FDA Drug Moderate Aug 21, 2013

Alprostadil IN NS Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Gentamicin Sulfate Irrigation, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Bacteriostatic Water for Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

3M Tekk Brand Industrial/Construction First Aid Kit, Total Resources Int'l Walnut, CA 91789

Total Resources Intl

FDA Drug Low Aug 21, 2013

Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Columbus, OH --- NDC 0054-0018-20

Boehringer Ingelheim Roxane Inc

FDA Drug Moderate Aug 21, 2013

REEVA (triclosan) Antibacterial Hand Soap and Dishwashing Liquid, Green Apple, 0.10%, 24 fl oz. bottle, Distributed by Aldi Inc,. Batavia, IL 60510; UPC 0 4198 1525 8.

Showline Automotive Products, Inc. dba US Soaps Mfg. Company

FDA Drug Moderate Aug 21, 2013

Acetylcysteine Ophthalmic Solution, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Testosterone Cypionate/Propionate Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Buprenorphine HCl Veterinary Injection, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

FDA Drug Moderate Aug 21, 2013

Nandrolone Decanoate Injectable, compounded by Pallimed Solutions Pharmacy, Woburn, MA

Pallimed Solutions

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2013

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 2013 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.