PlainRecalls

2013 Recalls

6,262 recalls · Page 47 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 1 critical, 48 moderate, and 1 lower-severity recalls. The page references 23 distinct recalling firms operating in 3 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (48), CPSC (1), 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 Sep 25, 2013

TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Suture: Part Number: 72202603 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the upper or lower jaw to provid…

Biomet 3i, LLC

FDA Devices Moderate Sep 25, 2013

Brilliance CT 6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N 728231, Philips Healthcare, Clevelan…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Sep 25, 2013

GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The angiography X-ray systems are indicated for use in generating fluoroscopi…

GE Healthcare, LLC

FDA Devices Moderate Sep 25, 2013

GE Healthcare, CARESCAPE Monitor B850. Intended for use in multiple areas within a professional healthcare facility.

GE Healthcare, LLC

FDA Devices Moderate Sep 25, 2013

Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measurement of axial eye length.

Sonogage Inc

FDA Devices Moderate Sep 25, 2013

3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing casts for either wet or dry…

3M Company - Health Care Business

FDA Devices Moderate Sep 25, 2013

ACL TOP 700; PN 0000280010 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the he…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202626 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

Vygon 14 Microbore Extension Set with Bionector, CMS-814-1. The CMS-814-1 is a 14 inch extension set used to administer IV fluids.

Churchill Medical Systems, Inc.

FDA Devices Moderate Sep 25, 2013

GE Healthcare, Advantage Workstation, READY View Application. Image analysis software.

GE Healthcare, LLC

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra PLLA/HA 5.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black: Part Number: 72202602 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

BIORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture; Part Number: 72200774 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

BIORAPTOR 2.9 mm Suture Anchor, pack of 1 ULTRABRAID Suture: 72200689 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra PLLA/HA 6.5 mm with 3 ULTRABRAID Suture; Part Number: 72202610 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241 Hyper-Hypothermia device used to …

Cincinnati Sub-Zero Products Inc

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra HA 6.5 mm with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202631 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

NX3 Try-In Gel. The product is used as a tooth shade resin material.

Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

FDA Devices Moderate Sep 25, 2013

POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access to the vascular system to sample blood and admin…

Access Scientific Inc

FDA Devices Moderate Sep 25, 2013

Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and general fluoroscopy proced…

Villa Radiology Systems LLC

FDA Devices Moderate Sep 25, 2013

ACL TOP CTS; PN 0000280020 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in the he…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

Cypher MIS Screw System, Biomet Spine Parsippany, NJ 07054. The Cypher MIS Screw System is a non-cervical spinal fixation device. 1)Screw Tower - RE…

Ebi, Llc

FDA Devices Moderate Sep 25, 2013

ACL TOP 700 CTS; PN 0000280050 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in th…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

BIORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture; Part Number: 72200775 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

Hemoccult II BRAND SENSA elite; MATERIALS AND REAGENTS; Hemoccult II SENSA elite Slides (Test Cares) containing guaiac paper; Hemoccult SENSA Develop…

Assuramed

FDA Devices Moderate Sep 25, 2013

Central Dressing Change Kit; AMS-8464CP- 6. Vygon Central Dressing Change Kit contains: 1 Pair Nitrile Gloves W/Wallet, Powderfree 1 Face Mask 1 Po…

Churchill Medical Systems, Inc.

FDA Devices Moderate Sep 25, 2013

T8 REMOVAL HEAD, REF 8910641, QTY: 1 EA, Product Usage: The non-sterile T8 Removal Diriver is used with the Spire and Spire Z Spinal System in c…

Medtronic Sofamor Danek USA Inc

FDA Devices Moderate Sep 25, 2013

RAPTORMITE" 3.7 mm PLLA with two ULTRABRAID" Sutures Size 0 and Needles; Part Number: 72201805 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

ACL TOP 300 and ACL TOP 300 CTS (Japan); PN 0000280060 Bench top, fully automated, random access analyzer designed specifically for in vitro diagn…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

BIORAPTOR 2.9 mm Suture Anchor with DURABRAID" Suture; Part Number: 72200783 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Low Sep 25, 2013

King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthe…

King Systems Corp.

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue; Part Number: 72202597 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Critical Sep 25, 2013

Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of primary and secondary fluids when p…

B Braun Medical, Inc.

FDA Devices Moderate Sep 25, 2013

OSTEORAPTOR 2.3 mm with 1 ULTRABRAID Suture, White; Part Number: 72201991 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

Laserworld RGB & Piko Nano RGB Models All models are laser light show projectors, and will be used as such.

Laserworld Usa Inc

FDA Devices Moderate Sep 25, 2013

C2244.3820;, CONELOG Titanium Base CC ¿3.8GH2.0 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be us…

Camlog Usa

FDA Devices Moderate Sep 25, 2013

C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 inkl HS Product Usage: Endosseous dental implant abutment CONELOG Abutments are intended to be use…

Camlog Usa

FDA Devices Moderate Sep 25, 2013

VisuALIF,System consisting of a 'U' shaped PEEK block in two footprint configurations, four heights and three lordosis angles., part number: 0301-14…

Spine Smith Holdings, LLC

FDA Devices Moderate Sep 25, 2013

GE Healthcare, CARESCAPE Monitor B650. The CARESCAPE Monitor B650 is a multi-parameter patient monitor intended for use in multiple areas and intr…

GE Healthcare, LLC

FDA Devices Moderate Sep 25, 2013

ACL TOP 500 CTS; PN 0000280040 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in th…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

ACL TOP 700 LAS; PN 0000280030 Bench top, fully automated, random access analyzer designed specifically for in vitro diagnostic clinical use in th…

Instrumentation Laboratory Co.

FDA Devices Moderate Sep 25, 2013

Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product Usage: Surgical placement in the upper or lower jaw to provide a means …

Biomet 3i, LLC

FDA Devices Moderate Sep 25, 2013

Cranial Access (CRAK) Kits, Product / Catalogue No.s: INSHITH, INSHITHND, INSHITHRZN The kits allow for access to the subarachnoid space or the la…

Integra LifeSciences Corp. d.b.a. Integra Pain Management

FDA Devices Moderate Sep 25, 2013

OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number: 72203291 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra 6.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID) with Needles; Part Number: 72202620 Biodegradable s…

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

TWINFIX" Ultra 4.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures (blue, blue-COBRAID") with Needles; Part Number: 72202612 Biodegradable…

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number: 72201993 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

FDA Devices Moderate Sep 25, 2013

TWINFIX Ultra HA 4.5 mm Suture Anchor with 2 ULTRABRAID Suture, Blue / Black; Part Number: 72202624 Biodegradable suture anchor

Smith & Nephew, Inc. Endoscopy Division

CPSC Moderate Sep 25, 2013

Votive Candle Holders Sold at Cracker Barrel Old Country Store Recalled Due to Fire Hazard; Made by Mercuries Asia

Mercuries Asia Ltd., of Taipei, Taiwan

NHTSA Moderate Sep 24, 2013

MAZDA 2009-2013: LATCHES/LOCKS/LINKAGES:DOORS:LATCH

MAZDA

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.