PlainRecalls

2013 Recalls

6,215 recalls · Page 113 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 50 records, severity classification shows 6 critical, 41 moderate, and 3 lower-severity recalls. The page references 32 distinct recalling firms operating in 4 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), FDA Drug (13), FDA Food (5), 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 Mar 6, 2013

Potato & Mushroom Dumplings, Net Weight 1 lb. (16 oz.), KEEP FROZEN, UPC 6 54368 10039 3 --- JS Pelmeni OK - EST # A615133 - 667 Coney Island Ave., …

Js Pelmeni Ok, Inc.

FDA Food Critical Mar 6, 2013

3 Bean Munchies sprouts is a mixture of Green Peas, Cow Peas, Red Lentils and Garbanzo Beans. Product is packaged in a 4 oz clamshell container and …

Giant Greens, Inc.

FDA Food Critical Mar 6, 2013

GoldCoast Salads Blue Crab Spread (8oz and 16oz in flexible plastic cup with flexible plastic lids - keep refrigerate at 38 or below)

GoldCoast Salads

FDA Food Critical Mar 6, 2013

Mung Bean sprouts is packaged in a 8 oz clamshell container or 5 lb. bag and sold under the Sprouters Northwest or Life Force brand. The Life Fo…

Giant Greens, Inc.

FDA Food Critical Mar 6, 2013

Sold as In-House brand iced tea: Garbanzo Mediterranean Grill Organic Lemongrass Ginger Green Tea, 3 oz. packages

Teatulia

FDA Drug Moderate Mar 6, 2013

Furosemide Injection USP (10 mg/mL), 4 mL in 5 mL Fliptop Vial, Rx only, Hospira Inc., Lake Forest, IL --- NDC 0409-6102-04

Hospira, Inc.

FDA Drug Moderate Mar 6, 2013

Citalopram tablets USP, 40mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-344-30

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 6, 2013

Belladonna Alkaloids (hyoscyamine sulfate, USP 0.1037 mg; atropine sulfate, USP 0.0194 mg; scopolamine HBr, USP 0.0065 mg) with Phenobarbital (USP 16…

West-ward Pharmaceutical Corp.

FDA Drug Moderate Mar 6, 2013

Citalopram tablets USP, 10mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-342-…

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 6, 2013

Dextroamphetamine Sulfate Extended Release Capsules, 5 mg, 90 capsules, Rx only, Manufactured by Catalent Pharma Solutions for CorePharma, LLC Middle…

Amedra Pharmaceuticals LLC

FDA Drug Moderate Mar 6, 2013

Dextroamphetamine Sulfate Extended Release Capsules, 5 mg, 90 capsules, Rx only, Manufactured by Catalent Pharma Solutions for CorePharma, LLC Middle…

Amedra Pharmaceuticals LLC

FDA Drug Moderate Mar 6, 2013

Dextroamphetamine Sulfate Extended Release Capsules, 5 mg, 90 capsules, Rx only, Manufactured by Catalent Pharma Solutions for CorePharma, LLC Middle…

Amedra Pharmaceuticals LLC

FDA Drug Moderate Mar 6, 2013

Citalopram tablets USP, 20mg, 30-count bottle, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli, India 502 325, NDC 55111-343-30

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 6, 2013

EXPAREL (bupivacaine liposome injectable suspension), 1.3%, 266 mg/20 mL (13.3 mg/mL) single use vials, INVESTIGATIONAL USE. For Infiltration Only. …

Pacira Pharmaceuticals, Inc.

FDA Drug Low Mar 6, 2013

Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400 mg/Expectorant, a) 24 coated caplets per blister pack, UPC 3002…

Bayer Healthcare, LLC

FDA Drug Moderate Mar 6, 2013

0.9% Sodium Chloride Irrigation, USP, 3000 mL, Sterile, Non pyrogenic, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7972-08

Hospira Inc.

FDA Drug Low Mar 6, 2013

buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg, 30 tablet bottles, Rx Only, NDC 67767-142-30 Actavis Distributed by: Actavis South At…

Actavis Pharmaceuticals

FDA Drug Moderate Mar 6, 2013

Isoniazid Tablets 300 mg tablets USP, Rx Only, a) 30 tablets - NDC 61748-013-30, b) 100 tablets - NDC 61748-013-01, Mfd for: VersaPharm Incorporated…

West-ward Pharmaceutical Corp.

FDA Devices Moderate Mar 6, 2013

Philips MX 16-Slice CT Scanner System, a whole-body computed tomography X-ray system.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

QuietCare-Networked product, Facility Server/model: QC101601; The QuietCare system is intended to detect and analyze residents' movements.

Intel-GE Care Innovations LLC

FDA Devices Moderate Mar 6, 2013

Philips Medical Systems, Brilliance Computed Tomography (CT) X-Ray Scanners, Big Bore, Model #728243; and Brilliance Computed Tomography (CT) X-Ray S…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

Stryker XIA 3 Iliac Screwdriver, 3-PCS. The XIA 3 Iliac Screwdriver is used to drive XIA 3 closed head Monoaxial and closed head Polyaxial screw…

Stryker Spine

FDA Devices Moderate Mar 6, 2013

Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake 10x; REF 454413. HE0396. greiner bio-one; 13x75 50pcs.,1200 pcs in total. …

Cellestis Inc

FDA Devices Moderate Mar 6, 2013

Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.

Myco Medical Supplies Inc

FDA Devices Moderate Mar 6, 2013

Versafitcup Impacting Ring Model Number: 01.26.10.0133 (46mm), 01.26.10.0134 (48mm), 01.26.10.0135 (50mm), 01.26.10.0136 (52mm), 01.26.10.0137 (54…

Medacta Usa Inc

FDA Devices Moderate Mar 6, 2013

Philips DigitalDiagnost X-Ray System with Eleva Software 2.1.3 Model numbers 712020, 712022, and 712082 Product Usage: Digital radiographi…

Philips Healthcare Inc.

FDA Devices Moderate Mar 6, 2013

Elekta, Apex add-on Micro MLC, collimator for radiation therapy.

Elekta, Inc.

FDA Devices Moderate Mar 6, 2013

Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in endoscopic surgery. For use when a rigid endoscopic instrument for grasp…

Integra LifeSciences Corp.

FDA Devices Moderate Mar 6, 2013

Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH 44143 The Brilliance Scanner a…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into a printed carton. Distributed by McNe…

Mc-NEIL-PPC, Inc.

FDA Devices Moderate Mar 6, 2013

GE Healthcare Definium 5000 / 5220493 X-Ray System

GE Healthcare, LLC

FDA Devices Moderate Mar 6, 2013

Philips Medical Systems, Extended Brilliance Workspace (EBW) X-Ray Scanners, Model #728260. A component of the Computed Tomography X-Ray System.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.

Aesculap, Inc.

FDA Devices Moderate Mar 6, 2013

REF CMS-CT6T225, 6F Triple Lumen CT PICC with M.S.T. Components Product Usage: Power injectable infusion PICC insertion kits

Medical Components, Inc dba MedComp

FDA Devices Moderate Mar 6, 2013

VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN; Shake 10x; REF 454074; HE0105; 13X75 50 pcs.,1200 pcs. in total; Product Usage: QuantiFERON¿-T…

Cellestis Inc

FDA Devices Moderate Mar 6, 2013

Advanced Neuromodulation Systems, Brio DBS System implantable neurostimulator, IPG or R-IPG, Model 6788 Implantable Pulse Generator.

Advanced Neuromodulation Systems Inc.

FDA Devices Moderate Mar 6, 2013

Philips Medical Systems, GEMINI TF Big Bore, Model #882476, Positron Emission Tomography (PET) and X-Ray Computed Tomography (CT) scanning system, a …

Philips Medical Systems (Cleveland) Inc

FDA Devices Low Mar 6, 2013

Avex CX Suite, Avex CX 0.22 UL4,5 HK REF #224-017, Product Usage: Avex CX ceramic brackets are formed with 99.9% pure alumina oxide. The indi…

Ultradent Products, Inc.

FDA Devices Moderate Mar 6, 2013

Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic Distractor. The ISKD is intended for limb lengthening of the tibia and fe…

Orthofix, Inc

FDA Devices Moderate Mar 6, 2013

KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is packaged in 2.5 oz bottles, which are then packed into a printed carton. Distri…

Mc-NEIL-PPC, Inc.

FDA Devices Moderate Mar 6, 2013

GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System

GE Healthcare, LLC

FDA Devices Moderate Mar 6, 2013

Ingenuity TF PET/CT. Diagnostic imaging system

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

GE Healthcare Definium 5000/5220493-2 X-Ray System

GE Healthcare, LLC

FDA Devices Moderate Mar 6, 2013

Philips Medical Systems, GEMINI LXL - Model #882412; GEMINI TF 16 - Model #882470 and Model #882473; GEMINI TF 64 - Model #882471, Positron Emission …

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 6, 2013

Atrapro Antipruritic Hydrogel, 1.5 oz gel tube, 4 Net wt/ 1.5 oz.. RX only, Professional Sample, Not for Sale. Pre-printed tube: MS31071, Shelf ca…

Oculus Innovative Sciences Inc

FDA Devices Moderate Mar 6, 2013

KY TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc.

Mc-NEIL-PPC, Inc.

FDA Devices Moderate Mar 6, 2013

BMC RF Cannula Curved Sharp RadiOpaque, Non-Pyrogenic, Active Tip: 10mm, Gauge 16 Ga, Length: 100mm. The BMC RF Cannula is sealed in a Tyvek pouch (…

Baylis Medical Company Inc.

FDA Devices Moderate Mar 6, 2013

Firebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod Connector (52-6700). Product Usage: The connector assemblies al…

Orthofix, Inc

NHTSA Critical Mar 6, 2013

KENWORTH 2014: SEAT BELTS

KENWORTH

CPSC Moderate Mar 5, 2013

Briggs & Stratton Recalls Ariens Compact Snow Blowers Due to Fire Hazard

Briggs & Stratton Corporation, of Milwaukee, Wis.

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