PlainRecalls

2013 Recalls

6,215 recalls · Page 125 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 15 records, severity classification shows 3 critical, 11 moderate, and 1 lower-severity recalls. The page references 13 distinct recalling firms operating in 3 distinct product categories, with 14 of 15 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (12), CPSC (2), NHTSA (1), 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 Jan 2, 2013

Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog no. D140010, Large Curve catalog no. D140011. The MobiCath Bi-Directio…

Greatbatch Medical

FDA Devices Moderate Jan 2, 2013

Stryker Howmedica Osteonics; Stryker T2 Humerus System Teflon Tube, sterile; REF 1806-0073S The T2 Nailing System is designed to treat complex fr…

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Jan 2, 2013

Diamigo i-Phone App The Diamigo app was intended for use as an educational tool in the management of diabetes.

sanofi-aventis US, Inc.

FDA Devices Moderate Jan 2, 2013

Brookstone Heated Body Bean, electrically heated SKU numbers: 734863 (Blue), 734864 (Plum), 734865 (Red). Brookstone 3 in 1 wrap ,SKU734397 (Brown…

Brookstone Company, Inc.

FDA Devices Critical Jan 2, 2013

GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal Patient Circuit Kit Disposable with Size 1 Mask***M1091335 QTY: 10 T-Pi…

GE Healthcare, LLC

FDA Devices Critical Jan 2, 2013

Zimmer Spine Ardis Inserter, Rx, non-sterile

Zimmer, Inc.

FDA Devices Moderate Jan 2, 2013

Access Immunoassay Systems Total T4 Calibrators, Part Number: 33805. The Access Total T4 Calibrators are intended to calibrate the Access Total …

Beckman Coulter Inc.

FDA Devices Low Jan 2, 2013

Qualicheck 1+, Aqueous Quality Control, Level 2, S7140, REF 944-042. The solution is used for quality check of blood gas analyzers.

Radiometer America Inc

FDA Devices Moderate Jan 2, 2013

COBAS AmpliPrep Instrument (CAP) with AMPLILINK (AL) Software v.3.3.5 Automated sample processing instrument used with CAP/CA and CAP/CTM. Roch…

Roche Molecular Systems, Inc.

FDA Devices Moderate Jan 2, 2013

Access Immunoassay System, Access 2 Immunoassay System, Synchron LXi 725 Clinical System, UniCel DxC 600i Synchron Access Clinical System Part…

Beckman Coulter Inc.

FDA Devices Moderate Jan 2, 2013

Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov, Sweden; Model 512003; a non-inva…

Arjo, Inc. dba ArjoHuntleigh

FDA Devices Moderate Jan 2, 2013

Computed Tomography X-Ray System, Extended Brilliance Workspace (EBW), Model #728260 Philips Healthcare, Highland Heights, OH The Extended Brilli…

Philips Medical Systems (Cleveland) Inc

CPSC Moderate Jan 2, 2013

Academy Sports + Outdoors Recalls Crossbow Cocking Ropes Due to Laceration Hazard

CPSC Moderate Jan 2, 2013

Brower Recalls Top Hatch Egg Incubators Due to Fire Hazard

Brower Division of Hawkeye Steel Products Inc., of Houghton, Iowa

NHTSA Critical Jan 2, 2013

CADILLAC,CHEVROLET,GMC 2013: STEERING:COLUMN LOCKING:ANTI-THEFT DEVICE

CADILLAC,CHEVROLET,GMC

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