2013 Recalls
6,262 recalls · Page 77 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 16 critical, 33 moderate, and 1 lower-severity recalls. The page references 32 distinct recalling firms operating in 7 distinct product categories, with 39 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), NHTSA (9), CPSC (7), 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.
Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. The pump…
Medtronic Neuromodulation
BD SafetyGlide Allergy. REF 305950 Sterile Allergy Treatment Syringe Tray. The device is used for aspiration and injection of medications.
Becton Dickinson & Company
DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs Monitor: Product Usage: Monitor, Physiological, Patient
Medrad Inc
Sarns " TCM II Temperature Control Module The Sarns" TCM II Temperature Control Module is a source of temperature-controlled water for blood heat …
Terumo Cardiovascular Systems Corporation
Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies. This product is used to alert caregivers when a patient at r…
RF Technologies, Inc.
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
Medtronic Sofamor Danek USA Inc
Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer Greatbatch Medical 2300 Berkshire Lane North, Minne…
Greatbatch Medical
Multilite Dye Handpieces, an optional accessory of the RevLite SI Laser. The Revlite SI laser is intended for General Dermatology, Dermatologic an…
ConBio, a CynoSure Company
Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems). Baxter's Infusor SV Elastomeric Infusion Device Device Listing: D0208…
Baxter Healthcare Corp.
Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E, QPC1721E and QFC1683E contain pr…
Steris Corporation
Brand Name: Multirate Infusor Devices. Indicated for the intravenous administration of medications.
Baxter Healthcare Corp.
Medtronic Intrathecal Catheter Pump Segment Revision Kit, model 8596SC. Contents: 60-cm pump segment with attached sutureless pump connector, Spina…
Medtronic Neuromodulation
CoaguChek XS Plus System The CoaguChek XS Plus system for use by professional healthcare providers for quantitative prothrombin time testing for t…
Roche Diagnostics Operations, Inc.
Brand Name: Multiday lnfusor, Seven Day lnfusor and the Basal/Bolus lnfusor: Single day Infusor 2 ml/h, Single Day INFUSOR 2 ml/h System, Hal…
Baxter Healthcare Corp.
Prism Medical C-Series Carry Bar, Class I, model number 360755. The intended use is a carry bar attached to a C-450 or C-625 ceiling lift used to…
Prism Medical Services USA
Medtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The SynchroMed EL Pumps are supplied in 10 ml or 18 ml reservoir size.)…
Medtronic Neuromodulation
CoaguChek XS System (HCP) The CoaguChek XS System is intended for use by professional healthcare providers for quantitative prothrombin time testi…
Roche Diagnostics Operations, Inc.
Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous administration of medications.
Baxter Healthcare Corp.
The Centricity Laboratory System is intended to be an information system designed to support the clinical and administrative activities associated wi…
GE Healthcare It
Brand Name: Infusor SV and LV Elastomeric Infusion Devices. Indicated for the intravenous administration of medications.
Baxter Healthcare Corp.
Brand Name: Basal/Bolus Infusor. Indicated for the intravenous administration of medications.
Baxter Healthcare Corp.
GE Healthcare Senographe Essential System. The Senographe 2000D system generates digital mamnmographic images that can be used for screening and i…
GE Healthcare, LLC
TRUE Dilatation Balloon Valvuloplasty Catheter, REF Numbers: 02045-11, 02245-12, 02445-12, and 02645-13; Sizes: 20mm x 4.5cm, 22mm x 4.5cm, 24m…
Loma Vista Medical
Medtronic SynchroMed II, Model 8637, (The SynchroMed II Pump is supplied in 20 ml or 40 ml reservoir size.) Sterilized using ethylene oxide. Pro…
Medtronic Neuromodulation
Soma v Automated Breast Ultrasound System (ABUS), Automated Breast Ultrasound. Indicated as an adjunct to mammography for breast cancer screening.
U-systems Inc
Medtronic INDURA 1P Intrathecal Catheter, model 8709SC. Contents: 81.4-cm catheter with length markers and guide wire, 15 T-gauge introducer needle…
Medtronic Neuromodulation
CMC Saddle Product Usage: The Ascension CMC is intended to resurface the proximal end of the first metacarpal in cases of rheumatoid arthritis, t…
Integra LifeSciences Corp.
INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
Medtronic Sofamor Danek USA Inc
Medtronic SynchroMed EL Programmable pumps, Models 8626, 8626L, 8627, 8627L, (The SynchroMed EL Pumps are supplied in 10 ml or 18 ml reservoir size.)…
Medtronic Neuromodulation
INFUSE(R) Bone Graft,LARGE II KIT, REF 7510800, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
Medtronic Sofamor Danek USA Inc
Angel’s Touch Collections Recalls Butterfly and Shell Lamps Due to Shock and Fire Hazards; Sold Exclusively at Cracker Barrel Old Country Store
Angel's Touch Collections Co., Ltd., of Rego Park, N.Y.
Outdoor Solutions Hammock and Sunshade Recalled by H-E-B Due to Fall Hazard
Toys R Us Recalls Remote-Controlled Helicopters Due to Fire and Burn Hazards
TOYOTA 2012: STEERING:ELECTRIC POWER ASSIST SYSTEM
TOYOTA
Yamaha Recalls Big Bear ATVs Due to Crash Hazard (Recall Alert)
Yamaha Motor Corporation USA, of Cypress, Calif.
CHRYSLER,DODGE 2013: AIR BAGS
CHRYSLER,DODGE
JEEP 2014: EXTERIOR LIGHTING
JEEP
RAM 2013: STRUCTURE
RAM
RAM 2013: ELECTRONIC STABILITY CONTROL (ESC)
RAM
CHRYSLER,DODGE,RAM 2013: ELECTRICAL SYSTEM
CHRYSLER,DODGE,RAM
CHRYSLER,DODGE,JEEP 2011-2013: ELECTRICAL SYSTEM
CHRYSLER,DODGE,JEEP
BMW 2013: ELECTRICAL SYSTEM
BMW
Fred & Friends Recalls Baby Rattles Due to Choking Hazard
Easy Aces, Inc. d/b/a Fred & Friends, of Cumberland, R.I.
Stile Products Recalls Tern Folding Bicycles Due to Fall Hazard
Alu Maga Industrial Co., Ltd., of Taiwan
Swan Creek Recalls Loose Votive Candles Due to Fire Hazard
Swan Creek Candle Co., of Swanton, Ohio
CHEVROLET 2012: ELECTRONIC STABILITY CONTROL (ESC)
CHEVROLET
vega one, all-in one nutrition bar; chocolate cherry flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, prob…
Sequel Naturals Ltd
vega one, all-in one nutrition bar; Double chocolate flavor Added vitamins and minerals; 15 g Protein, 6 g Fiber and 1.5 g Omega Antioxidants, pro…
Sequel Naturals Ltd
MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage, 15.2 oz plastic (PET) bottles, Produced for The Coca Cola Company, Atlanta, GA 30313 USA.
Coca-Cola Refreshments USA, Inc.
MINUTE MAID APPLE JUICE, 100% Juice, 6/10 oz and 15.2 oz, plastic (PET) bottles, Produced for The Coca Cola Company, Atlanta, GA 30313 USA.
Coca-Cola Refreshments USA, Inc.
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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.