PlainRecalls

2013 Recalls

6,262 recalls · Page 54 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 5 critical, 43 moderate, and 2 lower-severity recalls. The page references 29 distinct recalling firms operating in 6 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), FDA Food (14), NHTSA (3), 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 Devices Moderate Sep 4, 2013

Philips Easy Upgrade DR, Code No: 712086 This system is used for making X-Ray exposures for diagnostics.

Philips Healthcare Inc.

FDA Devices Low Sep 4, 2013

OLA Buffer For Laboratory Use; Contents: 1 tube with buffered solution containing MgCl2 (80 ¿M) and KCL (300 ¿M. 10.0ml.) PN: 50003300; Store a…

Celera Corporation

FDA Devices Moderate Sep 4, 2013

GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to be used in medical practices and in clinical departments and serves the purp…

GE Healthcare, LLC

FDA Devices Moderate Sep 4, 2013

PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers, Catalog Numbers LKPS1, LKPS5 and LKPTS1(D); and in the IMMULITE 2000/2000XPi Syst…

Siemens Healthcare Diagnostics

FDA Devices Moderate Sep 4, 2013

Pipeline Embolization Device (PED) The Pipeline Embolization Device is indicated for the endovascular treatment of adults (22 years of age and old…

Micro Therapeutics Inc, Dba Ev3 Neurovascular

FDA Devices Moderate Sep 4, 2013

PrepStain Tecan US-II. For use in the screening and detection of cervical cancer.

Becton Dickinson & Co.

FDA Devices Moderate Sep 4, 2013

SARKEN STAT! 1- Panel Test Kit-COC Product Usage- Labeled as FOR FORENSIC USE ONLY (Employee, Student or Probation Testing).

Sarken, Inc.

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/20, Stem size 04, prox. Stem dia. 20 mm, Length 250 mm, WALDEMAR LINK GmbH & CoKG, Barkhau…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

SARKEN STAT! 1- Panel Test Kit-OPI Product Usage: Labeled as FOR FORENSIC USE ONLY (Employee, Student or Probation Testing).

Sarken, Inc.

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0142/22, Stem size 005, prox. Stem dia. 22.5 mm, Length 210 mm, WALDEMAR LINK GmbH & CoKG, Bark…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

DeRoyal Insufflation Tubing sets: 1) REF 28-0206 Insufflation Tubing, Laparoscopic Rx Only 2) REF 28-0214 Hi-Flow Insufflation Tubing Rx Only 3) …

DeRoyal Industries Inc

FDA Devices Moderate Sep 4, 2013

Free Lock Femoral Hip Fixation System Compression Tube/Plate, different length (59, 75, 91, 107, 123 mm), holes (2, 3, 4, 5, 6) and degree angles (13…

Zimmer, Inc.

FDA Devices Moderate Sep 4, 2013

SpineNet Anterior Cervical Cage, Lordotic, Peek (originally submitted as Daytona Anterior Cervical Cage) Product Usage: Is indicated for use in s…

SpineNet

FDA Devices Moderate Sep 4, 2013

PrepStain AG. For use in the screening and detection of cervical cancer.

Becton Dickinson & Co.

FDA Devices Moderate Sep 4, 2013

Continuous Ventilator/Continuous Ventilator with Respiratory Mechanics, Model No. V1000

Respironics California Inc

FDA Devices Moderate Sep 4, 2013

Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Screw REF 604642S 4.0x42mm TL 14mm, sterile Pro…

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Sep 4, 2013

Axiom Artis systems. C-arm angiographic x-ray system x-ray, angiographic system.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0155/22, Stem size S-5, prox. Stem dia. 22.5 mm, Length 180 mm, WALDEMAR LINK GmbH & CoKG, Bark…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/12, Stem size 0, prox. Stem dia. 12 mm, Length 250 mm, WALDEMAR LINK GmbH & CoKG, Barkhaus…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx, Non sterile (sterilize before use) The Glenosphere Distractor must be…

Zimmer, Inc.

FDA Devices Moderate Sep 4, 2013

Synthes Trauma Nail System. The devices are indication for bone fixation.

Synthes USA HQ, Inc.

FDA Devices Moderate Sep 4, 2013

ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM DISTAL MEDIAL HUMERAL LOCKING PLATE, SHORT RIGHT 11 HOLES 178 MM LENGTH STERILE RX ONLY Produc…

Zimmer, Inc.

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/18, Stem size 03, prox. Stem dia. 18 mm, Length 250 mm, WALDEMAR LINK GmbH & CoKG, Barkhau…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0142/18, Stem size 003, prox. Stem dia. 18 mm, Length 210 mm, WALDEMAR LINK GmbH & CoKG, Barkha…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0155/18, Stem size S-3, prox. Stem dia. 18 mm, Length 180 mm, WALDEMAR LINK GmbH & CoKG, Barkha…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE, standard and short low profiles, several holes/length combinations (2/54, 3/70, 4/86, 5/1…

Zimmer, Inc.

FDA Devices Moderate Sep 4, 2013

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0155/12, Stem size S-0, prox. Stem dia. 12 mm, Length 180 mm, WALDEMAR LINK GmbH & CoKG, Barkha…

Waldemar Link GmbH & Co. KG (Corp. Hq.)

FDA Devices Moderate Sep 4, 2013

Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Double Dispense with software versions 3.5.1 and 3.6. In vitro diagnostic devic…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 4, 2013

GE Healthcare, TRAM MODULE, High-acuity patient monitoring. Product Usage: The TRAM Module is intended to provide uninterrupted monitoring of ph…

GE Healthcare, LLC

FDA Devices Moderate Sep 4, 2013

VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW, several length (55 mm to 155 mm), diameters (12.7 mm and 15.8 mm) and short thread, standard…

Zimmer, Inc.

NHTSA Critical Sep 4, 2013

TOYOTA 2006-2010: HYBRID PROPULSION SYSTEM: INVERTER

TOYOTA

NHTSA Critical Sep 4, 2013

LEXUS 2006-2011: ENGINE

LEXUS

CPSC Moderate Sep 3, 2013

Target Recalls Threshold Floor Lamps Due to Fire and Shock Hazard

J. Hunt & Company of Bono, Ark.

CPSC Moderate Aug 29, 2013

Build-A-Bear Recalls Stuffed Animal Toy Due to Choking Hazard

CPSC Moderate Aug 29, 2013

L.L.Bean Recalls Step Stools Due to Fall Hazard (Recall Alert)

L.L.Bean Inc., of Freeport, Maine

NHTSA Critical Aug 29, 2013

FORD,LINCOLN,MERCURY 2005-2011: STEERING

FORD,LINCOLN,MERCURY

FDA Food Moderate Aug 28, 2013

Texas Wild UPC, 10/15 BSO, Shrimp Headless Shell-on, IQF, Wild Caught, Product of USA, 20# Net Weight, Galveston Shrimp Co., Galveston, TX 77550

Galveston Shrimp Company, Inc.

FDA Food Low Aug 28, 2013

Okami Fully Cooked Wild-Caught Lobster Roll with Avocado, in a 7oz plastic tray with lid, to be stored less than or equal to 40 degrees F.

Green Core

FDA Food Moderate Aug 28, 2013

Maple flavored lipid-based inclusions. Maple NT-RF and Maple NT-MF, NET WT: 50 lbs, Ingredients: Sugar, vegetable oil (palm, palm kernel), wheat flo…

SensoryEffects Powder Systems

FDA Food Moderate Aug 28, 2013

Plum Organics Mighty 4 Essential nutrition blend; Pumpkin Pomegranate Quinoa, Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. Selli…

Plum Inc

FDA Food Moderate Aug 28, 2013

Plum Organics Mighty 4 Essential nutrition blend; Purple Carrot Berry Quinoa, Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. Selli…

Plum Inc

FDA Food Moderate Aug 28, 2013

Texas Wild UPC, 16/20 WSO, Shrimp Headless Shell-on, IQF, Wild Caught, Product of USA 20# Net Weight, Galveston Shrimp Co., Galveston, TX 77550

Galveston Shrimp Company, Inc.

FDA Food Moderate Aug 28, 2013

Texas Wild UPC, 16/20 BSO, Shrimp Headless Shell-on, IQF, Wild Caught, Product of USA, 20# Net Weight, Galveston Shrimp Co., Galveston, TX 77550

Galveston Shrimp Company, Inc.

FDA Food Moderate Aug 28, 2013

Penguinos - four cream filled chocolate cupcakes: gluten, wheat & dairy free & vegan; 4 x 2.2oz cupcakes, net wt 8.8 oz. Ingredients: organic unre…

Mariposa Baking Co.

FDA Food Critical Aug 28, 2013

NuGo Free Dark Chocolate Trail Mix Bar, 1.59 oz (45g) Non-Dairy

NuGo Nutrition HQ

FDA Food Critical Aug 28, 2013

NuGo Dark Peanut Butter Cup, 1.59 oz (45g) Non-Dairy

NuGo Nutrition HQ

FDA Food Moderate Aug 28, 2013

Thai Chili Flake

Pacific Pure Aid

FDA Food Moderate Aug 28, 2013

Plum Organics Mighty 4 Essential nutrition blend; Sweet Potato Blueberry Millet , Greek yogurt in 4 oz pouch. Six pouches per box. USDA Organic. S…

Plum Inc

FDA Food Moderate Aug 28, 2013

Acidified Tea in a glass bottle with a multi-colored, stick-on label that reads in part: " HARMONY Chai Decaffeinated Fresh brewed on Orcas Island,…

Harmony Chai

FDA Food Moderate Aug 28, 2013

Texas Wild UPC 51/60 BSO Shrimp Headless Shell-on IQF, Wild Caught, Product of the USA 20 # Net Weight, Galveston Shrimp Co., Galveston, TX 77550

Galveston Shrimp Company, 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 July 2026.