PlainRecalls

2013 Recall Year Insight

Federal agencies issued 6,262 product recalls indexed by PlainRecalls in calendar year 2013. That represents about 6.00% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.2 recalls per day across the FDA, CPSC, USDA FSIS, 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 12 critical, 38 moderate, and 0 lower-severity recalls. The page references 30 distinct recalling firms operating in 5 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (28), FDA Food (10), NHTSA (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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Aug 7, 2013

Mesa Smart-Read EZTEST BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in determining the efficacy of steam sterilization processes.

Mesa Laboratories, Inc., Bozeman Manufacturing Facility

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 10 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration.

Hospira Inc.

FDA Devices Moderate Aug 7, 2013

uTASWako DCP, Lot TG340 2013.11, REF 995-60701, Wako Pure Chemical Industries, Ltd. 1-2 Doshomachi 3-chome, Chuo-Ku Osaka 540-8605 Japan Distributed by Wako Diagnostics Wako Life Sciences, Inc. 1025 Terra Bella Ave., Suto A. Mountain View, CA 94043 USA. The product is a single reagent cartridge run on an automated system and each assay performed on a single disposable chip using microfluidic electrophoretic separation. The reagent cartridge contains various buffers and antibodies.

Wako Life Sciences, Inc.

FDA Devices Moderate Aug 7, 2013

Cardinal BI Stat Biological Test Pack with Instant Readout Integrator, SteriTec Product Code PL 160/A, Distributor Product Code T40311PE SteriTec Steam Biological Test Packs with Instant Readout Integrator Card: The Steam Biological Test Pack with Instant Readout Integrator is a steam sterilization monitor designed specifically for biological testing of pre-vacuum steam sterilizers operating at 132¿C (270¿F) for 3 minutes or longer. The Instant Readout Integrator Card gives the operator a pre

Steritec Products Mfc. Co., Inc.

FDA Devices Moderate Aug 7, 2013

GE Healthcare, LOGIQ e Ultrasound System. The LOGIQ i/e and Vivid e is a general purpose ultrasound system intended for use by a qualified physician for evaluation by ultrasound imaging or fluid flow analysis of the human body. Specific clinical applications and exam types include: Fetal/OB; Abdominal (GYN & Urology); Pediatric; Small Organ (breast, testes, thyroid); Neonatal and Adult Cephalic; Cardiac (adult & pediatric); Peripheral Vascular; Intra-operative (abdominal, thoracic and PV), M

GE Healthcare, LLC

FDA Devices Moderate Aug 7, 2013

Picis ED Pulsecheck - EMR Software Application - 2125, Software Versions: 5.2 and 5.3. The application stores patient information in a database, and it may analyze and/or display the data in different formats for evaluation by healthcare professionals for informational purposes.

Picis Inc.

FDA Devices Moderate Aug 7, 2013

EZTest Steam Biological Indicator, SteriTec Product Code EZS and EZS-400 EZTest Steam Biological Indicator: Mesa EZTest Steam Biological Indicator is a self contained Biological Indicator intended for monitoring the efficacy of 121¿C, 132¿C, 134¿C and 135¿C steam sterilization cycles. Mesa EZTest has a recommended incubation time of 24 hours.

Steritec Products Mfc. Co., Inc.

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 8.5 x 24 mm, Syringe volume 12 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

Mesa EZtest BIOLOGICAL INDICATOR MONITORING SYSTEM. Intended for use in determining the efficacy of steam sterilization processes.

Mesa Laboratories, Inc., Bozeman Manufacturing Facility

FDA Devices Moderate Aug 7, 2013

Exactech Articulated Driver A nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.

Exactech, Inc.

FDA Devices Moderate Aug 7, 2013

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)

HeartWare Inc

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 12 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

AU5800 Clinical Chemistry Analyzer with Automation Ready Connection (All Software Versions), Model Numbers AU5811, AU5821, AU5831 and AU5841. This system is for in vitro diagnostic use only.

Beckman Coulter Inc.

FDA Devices Moderate Aug 7, 2013

ViSi Mobile Monitor, Catalog No. 92-10010 The ViSi Mobile Monitoring System is intended for use by clinicians and medically qualified personnel for single or multi-parameter vital signs monitoring of adult patients.

Sotera Wireless, Inc.

FDA Devices Moderate Aug 7, 2013

Medline Med-Checks BI Test packs with Instant Readout Integrator, SteriTec Product Code PL 200, Distributor Product Code MDS200500IR SteriTec Steam Biological Test Packs with Instant Readout Integrator Card: The Steam Biological Test Pack with Instant Readout Integrator is a steam sterilization monitor designed specifically for biological testing of pre-vacuum steam sterilizers operating at 132¿C (270¿F) for 3 minutes or longer. The Instant Readout Integrator Card gives the operator a predict

Steritec Products Mfc. Co., Inc.

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 14 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

syngo Dynamics Information System (sDIS) versions 9.5 and VA10A. The syngo¿ Dynamics system is intended for the acceptance, transfer, display, storage, archive, and manipulation of digital medical images, including quantification and reportgeneration. syngo¿ Dynamics is not intended to be used for reading mammography images.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 7, 2013

Getinge Assure Accufast BI Test Pack w/ 5 Controls, SteriTec Product Code PL 395, Distributor Product Code 61301606638 The Smart-Read Biological Test Pack with Instant Readout Integrator: is designed specifically for biological testing of 3 or 4 minutes or longer at 132 (270 and 3 minutes at 135 pre-vacuum steam sterilizers.

Steritec Products Mfc. Co., Inc.

FDA Devices Moderate Aug 7, 2013

S-LIFT Slap Hammer, Part Number: 11-50204, Revision A The slap hammers are used primarily to remove trial instruments that are used to estimate sizes of intervertebral body fusion devices intended to promote fusion. These devices were used in conjunction with lumbar intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients.

SpineFrontier, Inc.

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 16 x 40 mm, Syringe volume 12 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

BD Affirm VPIII Microbial Identification Tests, packaged in kits, 120 test\kit, Catalog # 446257 and 24 test\kit, Catalog # 446252; kits are labeled in part ***Becton, Dickinson and Company, 7 Loveton Circle Sparks, MD 21152 USA, 800-638-8663, www.bd.com/ds*** The Affirm VPIII Microbial Identification Test is a DNA probe test intended for use in the detection and identification of Candida species,

Becton Dickinson & Co.

FDA Devices Moderate Aug 7, 2013

Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 MM ISSYS LP Screw Rx Non-Sterile. Custom Spine, Inc. 9 Campus Dr. Parsippany, NJ 07054 USA. TEL: 973-808-0019 The ISSYS LP Spinal Fixation System is intended to help provide immobilization and stabilization of spinal segments as an adjunct to fusion of the lumbar and/or sacral spine for pedicular and non-pedicular fixation.

Custom Spine, Inc.

FDA Devices Moderate Aug 7, 2013

Synthes Synapse SD Drill Guide, Part Number SD389.477, Lot Number 6913900 Indicated for Hooks, Plate/Rods, Rods and Screws when intended to promote fusion of the cervical spine fusion of the cervical spine and occipitocervical junction (occiput-T3), the plate/rod, rod, hook and screw (3.2 mm cortex) components of the Synthes Cervifix; Axon and Synapse Systems are indicated for the following: -Degenerative Disk Disease (DDD) (defined as neck pain of discogenic origin with degeneration of the d

Synthes USA HQ, Inc.

FDA Devices Moderate Aug 7, 2013

GAMMA3 System Long Nail Kit, R2.0, Ti, Left Distributed in USA by Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah, NJ 07430 USA A single use device intended for the temporary fixation, correction of stabilization of the right femur. The kit consists of intramedullary nail and set screw. The kit is used in combination with lag screw and (distal) locking screws and end cap as well.

Stryker Howmedica Osteonics Corp.

FDA Devices Moderate Aug 7, 2013

Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a modular tissue processor for the following laboratory applications: fixation, dehydration, infiltration with intermedium, and the paraffin infiltration of histological tissue specimens.

Leica Microsystems, Inc.

FDA Devices Moderate Aug 7, 2013

Inspira AIR Balloon Dilation system. Size 7 x 24 mm, Syringe volume 6-8 cc. Dilation of airway tree.

Acclarent, Inc.

FDA Devices Moderate Aug 7, 2013

GE Healthcare, VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM. The device is a general purpose ultrasound system. Specific clinical applications remain the same as previously cleared: Fetal/OB; Abdominal (including GYN, pelvic and infertility monitoring/follicle development); Pediatric; Small Organ (breast, testes, thyroid etc.); Neonatal and Adult Cephalic; Cardiac (adult and pediatric); Musculo-skeletal Conventional and Superficial; Peripheral Vascular; Transvaginal; Transrecta

GE Healthcare, LLC

CPSC No agency class Aug 7, 2013

LSI Recalls Wind Speed Sensors Due to Risk of Injury from Impact (Recall Alert)

Load Systems International, of Quebec, Canada

CPSC No agency class Aug 7, 2013

Toysmith Recalls Toy Light-Up Frogs and Ducks Due to Choking Hazard; Sold Exclusively at Cost Plus World Market

NHTSA No agency class Aug 7, 2013

BMW 2009-2010: FUEL SYSTEM, DIESEL: PRE-HEATER

BMW

NHTSA No agency class Aug 7, 2013

TOYOTA 2005-2011: SEAT BELTS

TOYOTA

CPSC No agency class Aug 6, 2013

Gerber Recalls Uppercut Knife and Sheath Sets Due to Laceration Hazard

CPSC No agency class Aug 6, 2013

Sleepharmony Pink Youth Beds Recalled by Glideaway Due to Violation of Lead Paint Standard

NHTSA No agency class Aug 6, 2013

CHEVROLET,GMC 2014: SERVICE BRAKES, HYDRAULIC

CHEVROLET,GMC

NHTSA No agency class Aug 5, 2013

JAGUAR 2013: ENGINE AND ENGINE COOLING

JAGUAR

NHTSA No agency class Aug 5, 2013

JAGUAR 2011-2014: ELECTRICAL SYSTEM

JAGUAR

CPSC No agency class Aug 1, 2013

Cannondale Recalls Slice RS Bikes Due to Fall Hazard (Recall Alert)

NHTSA No agency class Aug 1, 2013

SUBARU 2013-2014: POWER TRAIN:AUTOMATIC TRANSMISSION

SUBARU

NHTSA No agency class Aug 1, 2013

FORD 2012-2013: EXTERIOR LIGHTING

FORD

FDA Food Moderate Jul 31, 2013

Jacqueline's GOURMET COOKIES Raspberry Burst Cookies, Net Wt. 11 oz (8 units in total) packed in clear plastic with white labeling---Shelf life is 12 months frozen and 7 days after baked.

Price Chopper Golub Corperisable Warehouse

FDA Food Moderate Jul 31, 2013

Smart Sense Fruit & Granola Trail Mix, Net WT 4.0 oz , UPC 8 83967 29091 8, Distributed by Kmart corporation, Hoffman Estates, Il 60179, Minneapolis, MN 55414.

American Importing Co, Inc

FDA Food Moderate Jul 31, 2013

Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name: Donut House K -Cup Packs. 12-Count Retail Boxes, Product Code #8934, Donut House Decaffeinated K-Cup Packs

Green Mountain Coffee Roasters

FDA Food Moderate Jul 31, 2013

Orchard Reserve, Fiber Health Blend, Net WT 6.5 oz , UPC 0 71725 74211 7, Distributed by Amport Foods, Minneapolis, MN 55414.

American Importing Co, Inc

FDA Food Critical Jul 31, 2013

600910 PISTACHIOS SPLITS RAW 30#, UPC 2052600910

Bergin Fruit And Nut Co Inc

FDA Food Critical Jul 31, 2013

600943 PISTACHIOS KERNELS RAW 8/11 OZ SQ TUB, UPC 2052600943 601902 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG, UPC 2052601902 601902.09 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG BYERLYS, UPC 2052601902 600899 PISTACHIOS KERNELS RAW 30#, IUPAC 600901 PISTACHIOS KERNELS RAW 5#, UPC 2052600901 600900.05 PISTACHIOS KERNELS RAW 12/16 BAGLINE FESTIVAL, UPC 2052600900. 601902.08 PISTACHIOS KERNELS RAW 10/14 OZ TAPE BAG LUNDS RAW PISTACHIO KERNELS, UPC 2052601902.

Bergin Fruit And Nut Co Inc

FDA Food Critical Jul 31, 2013

601911 PISTACHIO KERNELS HOT & SPICY 30#, UPC 2052601911 601913 PISTACHIOS HOT AND SPICY 12/5 OZ BERGIN RED BAG, UPC 2052601913

Bergin Fruit And Nut Co Inc

FDA Food Critical Jul 31, 2013

Dried Oregano, cut and sifted; Organic; Product of Turkey, sold in 25 lb boxes High Quality Organics, Reno, NV

High Quality Organics, Inc.

FDA Food Critical Jul 31, 2013

601041 HEALTHY HEART MIX 12/14 OZ TRAY, UPC 2052601041 601078 HEALTHY HEART MIX 12/8 OZ CLAMSHELL, UPC 2052601078 601078.03 HEALTHY HEART MIX 12/8 OZ CLAMSHELL KOWALSKI, UPC 2052601078 601089 HEALTHY HEART MIX 16/6 OZ CLAMSHELL, UPC 2052601089 601089.1 HEALTHY HEART MIX 16/6 OZ CLAMSHELL CUB, UPC 1115099868 601125 HEALTHY HEART MIX 8/10 OZ SQ TUB, UPC 2052601125 601125.04 HEALTHY HEART MIX 8/10 OZ SQ TUB BOULDER, UPC 2052601125 601125.05 HEALTHY HEART MIX 8/10 OZ SQ TUB FEST

Bergin Fruit And Nut Co Inc

FDA Food Critical Jul 31, 2013

600908.03 PISTACHIOS KERNELS R/S 12/16 OZ TRAY KOWALSKI, UPC 2052600908 600909 PISTACHIOS KERNELS R/S 16/7 OZ CLAMSHELL, UPC 2052600909 600909.03 PISTACHIOS KERNELS R/S 16/7 OZ CLAMSHELL KOWALSKI, IUPAC 600904 PISTACHIOS KERNELS R/S 30#, UPC 2052600904 600905 PISTACHIOS KERNELS R/S 5#, UPC 2052600905 600906 PISTACHIOS KERNELS R/S 12/16 OZ BAGLINE, IUPAC.

Bergin Fruit And Nut Co 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2013

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2013 across the FDA, CPSC, USDA FSIS 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 September 2026.