PlainRecalls

2013 Recalls

6,262 recalls · Page 66 of 126

2013 Recall Year Insight

Federal agencies issued 6,262 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 6.16% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 17.2 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 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 11 critical, 36 moderate, and 3 lower-severity recalls. The page references 32 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 Devices (30), FDA Drug (11), FDA Food (9), 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 Jul 24, 2013

Item # H996189 Mango Diced 1/2" 5 LB, Ingredients: Mango Packed By: Riley's Dallas, Texas 75226 Product of Mexico

MR Cuts, L.p.

FDA Food Moderate Jul 24, 2013

Talenti Gelato, Toasted Almond, One Pint (473ml), Crafted by: Talenti, Marietta, GA 30062

Talenti Gelato

FDA Food Critical Jul 24, 2013

RAW SUNFLOWER KERNEL, DARK RAISIN 50/50 MIX 24/l0 oz packaged in clear plastic wrap.

Windy Acres Candy & Nut, Outlet Inc.

FDA Food Critical Jul 24, 2013

QFC Chicken Pesto Panini wrapped in polywrap packaging, 10.32 oz. in size, included with five (5) other types of sandwiches in a 6-count "variety pac…

Kroger Co

FDA Food Critical Jul 24, 2013

Broccoli Salad Kit with Dressing; packaged in plastic bags inside paper cartons, 5 bags per case.

Fresh Unlimited Inc

FDA Food Critical Jul 24, 2013

Item # H175455 Mango Sliced 2/2.5 LB and 5 LB, Ingredients: Mango Packed By: Riley's Dallas, Texas 75226 Product of Mexico

MR Cuts, L.p.

FDA Food Critical Jul 24, 2013

Broccoli Salad Kit No Dressing, No Bacon; packaged in plastic bags inside paper cartons, 4 bags per case.

Fresh Unlimited Inc

FDA Food Critical Jul 24, 2013

Broccoli Salad Kit No Dressing, packaged in plastic bags inside paper cartons, 4 bags per case.

Fresh Unlimited Inc

FDA Food Critical Jul 24, 2013

Item # 2999 Mango Chunks 2/5 LB, Ingredients: Mango Packed By: Riley's Dallas, Texas 75226 Product of Mexico

MR Cuts, L.p.

FDA Drug Moderate Jul 24, 2013

Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, Sodium Bicarbonate U.S.P. No. 4 Granular, Net Wt. 50 lbs. (22.68 kg.) per bag, Manufactured by…

Church & Dwight Inc

FDA Drug Low Jul 24, 2013

Medroxyprogesterone acetate, micronized (EP, USP) active pharmaceutical ingredient, Rx only, packaged in 6.0 kg drums (labeled as 6,000 kg), Bayer Sc…

Bayer HealthCare Pharmaceuticals Inc.

FDA Drug Moderate Jul 24, 2013

Oxytocin Injection, USP, (Synthetic), 10 USP Units/mL, for IV Infusion or IM Use, Rx Only, 1 mL vial, APP ) 10 USP Units/mL, 1 mL, APP Pharmaceutical…

Fresenius Kabi USA, LLC

FDA Drug Moderate Jul 24, 2013

Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP1 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 46…

Church & Dwight Inc

FDA Drug Critical Jul 24, 2013

Piperacillin and Tazobactam for Injection, USP, 40.5 grams per Pharmacy Bulk Package vial, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd., Irun…

Apotex Corp.

FDA Drug Moderate Jul 24, 2013

QUETIAPINE Fumarate Tablets 25mg 100 Tablets (10x10) Blister card, Rx, Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217,…

American Health Packaging

FDA Drug Moderate Jul 24, 2013

Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP5 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 46…

Church & Dwight Inc

FDA Drug Moderate Jul 24, 2013

Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP3 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 46…

Church & Dwight Inc

FDA Drug Low Jul 24, 2013

Amoxicillin for Oral Suspension, USP 200 mg/5 mL, a) 75 mL bottle NDC 0093-4160-78 and b) 100 mL bottle NDC 0093-4160-73, Rx Only, Manufactured in C…

Teva Pharmaceuticals USA, Inc.

FDA Drug Moderate Jul 24, 2013

Estarylla (Norgestimate and Ethinyl Estradiol) Tablets. USP, 0.25mg/0.035mg, 3X28 tablets per carton. Rx only, Manufactured by Laboratorios Leon Fa…

Sandoz Incorporated

FDA Drug Moderate Jul 24, 2013

Sodium Bicarbonate Powder, CAS-144-55-8, Arm & Hammer, labeled as a) USP2 Grade, packaged in bags of various quantities, Church & Dwight Co, Inc., 46…

Church & Dwight Inc

FDA Devices Moderate Jul 24, 2013

Edwards Lifesciences Suction Wand, models S099 and S0998B Suction wands are intended for hand held use and pericardial sumps are intended for stat…

Edwards Lifesciences, LLC

FDA Devices Moderate Jul 24, 2013

RemB Electric Universal Driver REF 6400-099-000 For use with the CORE and TPS System sRx Only The RemB Electric Universal Driver is intended for…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 24, 2013

LifeShield; Sterile; Rx only; List No. 19666-28; SYMBIQ PUMP SET, CONVERTIBLE PIN, PIGGYBACK, 2 CLAVES PORTS AND OPTION LOK, NON-DEHP; NOMINAL LENGTH…

Hospira Inc.

FDA Devices Moderate Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial blood parameter module. Intended for use during cardiopulmonary bypass procedures when con…

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Jul 24, 2013

MedStream Programmable Infusion Pump- Implantable for the intrathecal delivery of Baclofen or Morphine Product Code:91-4200 (20ml pump) US 91-4200. …

Codman & Shurtleff, Inc.

FDA Devices Moderate Jul 24, 2013

Various types of Fetal Bovine Serum Bovine sourced Animal Sera for in-vitro diagnostic device and as a growth promoting nutrient in cell culture s…

Paa Laboratories Inc

FDA Devices Moderate Jul 24, 2013

nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years of age or older in whom a cataractous lens has been removed by cataract extr…

Staar Surgical Co.

FDA Devices Moderate Jul 24, 2013

Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Usage: Eon: Eon system is indicated as an aid in the management of chronic intra…

St. Jude Medical

FDA Devices Moderate Jul 24, 2013

ExactaMix 1200 and 2400 Compounders. Used as an automated pumping system that compounds multiple sterile ingredients into a finished solution.

Baxa Corporation

FDA Devices Moderate Jul 24, 2013

KRD1 PedFuse Rods, Model: IM80100-13 Rev B Product Usage: Pedicle rods are cylindrical rods which act as a linking mechanism between pedicle scr…

SpineFrontier, Inc.

FDA Devices Moderate Jul 24, 2013

Safety Lancets - Odyssey, Button Activated; Tri- Bevel Tip for Virtually Painless Sampling; Needle automatically retracts, No lancing device requir…

KooJoo Trading Company

FDA Devices Moderate Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial blood parameter modules and Hematocrit/Saturation probe. Intended for use during cardiopu…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Venous blood parameter module. Intended for use during cardiopulmonary bypass procedures when conti…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation probe. Intended for use durin…

Terumo Cardiovascular Systems Corporation

FDA Devices Low Jul 24, 2013

TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information Syst…

Technidata S.A.

FDA Devices Moderate Jul 24, 2013

Polarizer D Fixed w/Rotating Red 1 lambda plate. Utilized in upright Zeiss microscopes to aid in diagnosis by means of color variation.

Zeiss, Carl Inc

FDA Devices Moderate Jul 24, 2013

Synthes CMF Distraction System The product is intended for use as a bone stabilizer and lengthening (and/or transport) device for correction of co…

Synthes USA HQ, Inc.

FDA Devices Moderate Jul 24, 2013

Afinity CQ2015A Intraocular Lens The visual correction of aphakia in persons 60 years of age or older in whom a cataractous lens has been removed …

Staar Surgical Co.

FDA Devices Moderate Jul 24, 2013

Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the Multi Vector Distractor which cis used for mandibul…

Synthes USA HQ, Inc.

FDA Devices Moderate Jul 24, 2013

Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus Product Usage: Angiographic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 24, 2013

Alair Bronchial Thermoplasty Catheter, Bronchial Thermoplasty System; Material Number: M005ATS25010, Catalog Number: ATS 2-5. Product is manufactured…

Boston Scientific Corporation

FDA Devices Moderate Jul 24, 2013

27023WU Balloon Catheter, 3 Fr., 2/pkg, sterile, contains latex. The RUSCH ureter occlusion catheter is indicated for the routine occlusion of t…

Karl Storz Endoscopy America Inc

FDA Devices Moderate Jul 24, 2013

CORE Universal Driver REF 5400- 99 Rx Only This drill may also be used with theTotal Performance System (TPS").The Stryker Total Performance Syste…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 24, 2013

Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem Company. The System is used in radiologic imaging procedures.

Leibel-Flarsheim Company LLC

FDA Devices Moderate Jul 24, 2013

Integra PANTA Arthrodesis Nail System. Intended for use in tibiotalocalcaneal arthrodesis and treatment of trauma to the hindfoot and distal tibia.

Integra LifeSciences Corporation

FDA Devices Moderate Jul 24, 2013

Eon Mini - 3721 (Charger). Product Usage: Eon Mini system is indicated as an aid in the management of chronic intractable pain of the trunk and…

St. Jude Medical

FDA Devices Moderate Jul 24, 2013

Stryker TPS Universal Driver REF 5100- 99 Rx , The Stryker Total Performance System (TPS) is intended for use in the cutting, drilling, reaming, d…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate Jul 24, 2013

B-CrossLaps/serum (B-CTx in serum) REF 11972308 160 100 tests Immunoassay for the in vitro quantitative determination of degradation products o…

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Jul 24, 2013

CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules. Intended for use during cardiopulmonary bypass procedure…

Terumo Cardiovascular Systems Corporation

FDA Devices Critical Jul 24, 2013

MedStream Programmable Infusion Pump , Implantable for the intrathecal delivery of Baclofen or Morphine Product Code: 91-4201US (40ml pump) 91-420…

Codman & Shurtleff, 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

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 2013 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.