PlainRecalls

2019 Recalls

7,396 recalls · Page 89 of 148

2019 Recall Year Insight

Federal agencies issued 7,396 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 8.81% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.3 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 148 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 2019.

On this page of 50 records, severity classification shows 16 critical, 30 moderate, and 4 lower-severity recalls. The page references 33 distinct recalling firms operating in 5 distinct product categories, with 38 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), NHTSA (11), FDA Food (9), 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 2019 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 Drug Moderate Jun 19, 2019

Sn-DMSA solution, Store Frozen, Not for Direct Injection, Synthetopes, Inc.

Synthetopes Inc

FDA Drug Moderate Jun 19, 2019

Biscolax Laxative (Bisacodyl, USP 10 mg), a) 12 suppositories per carton, NDC: 0904-5058-12, b) 100 suppositories per carton, NDC: 0904-5058-60, Dist…

Torrent Pharma Inc

FDA Devices Low Jun 19, 2019

CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage: Indications for Use: - Temporary left at…

Cardiocommand Inc.

FDA Devices Moderate Jun 19, 2019

Prestilix 1600X Prestilix system is a fully integrated remote controlled digital radiology system. It is designed for all general radiology appl…

GE Healthcare, LLC

FDA Devices Moderate Jun 19, 2019

Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote controlled system.

GE Healthcare, LLC

FDA Devices Critical Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The IntraClude intra-aortic occlusi…

Edwards Lifesciences, LLC

FDA Devices Moderate Jun 19, 2019

Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-saving des…

GE Healthcare, LLC

FDA Devices Moderate Jun 19, 2019

Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in hea…

Skytron, Div. The KMW Group, Inc

FDA Devices Moderate Jun 19, 2019

Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series Medical Washer-Disinfector i…

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Jun 19, 2019

Proteus XR/a The Proteus XR/a radiographic system offers the flexibility to choose a configuration based upon your specific requirements. The sys…

GE Healthcare, LLC

FDA Devices Moderate Jun 19, 2019

Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT

Cook Inc.

FDA Devices Moderate Jun 19, 2019

xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasiti…

Luminex Molecular Diagnostics

FDA Devices Moderate Jun 19, 2019

Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product Usage: The Getinge 86 Series Medical Washer-Disinfector is desig…

Maquet Cardiovascular Us Sales, Llc

FDA Devices Moderate Jun 19, 2019

GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d…

GE Healthcare, LLC

FDA Devices Moderate Jun 19, 2019

Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI 00886799000588. Used in card…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Jun 19, 2019

Conformis iTotal Hip Replacement System: HBS-033-00xx-010101, (HIP-PATIENT SPECIFIC STEM LEFT)

Conformis, Inc.

FDA Devices Low Jun 19, 2019

Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.01 (or la…

Philips North America, LLC

FDA Devices Moderate Jun 19, 2019

Conformis iTotal Hip Replacement System: HBS-033-00xx-020101, (HIP-PATIENT SPECIFIC STEM RIGHT)

Conformis, Inc.

FDA Devices Moderate Jun 19, 2019

InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician applicatio…

Medtronic Neuromodulation

FDA Devices Low Jun 19, 2019

Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Cent…

Philips North America, LLC

FDA Devices Moderate Jun 19, 2019

Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluorosco…

GE Healthcare, LLC

NHTSA Critical Jun 19, 2019

AUDI 2015-2019: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION

AUDI

NHTSA Moderate Jun 19, 2019

AUDI 2019: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

AUDI

NHTSA Critical Jun 19, 2019

BMW 2008-2012: ELECTRICAL SYSTEM:WIRING:FUSES AND CIRCUIT BREAKERS

BMW

CPSC Moderate Jun 18, 2019

Home Meridian Recalls Corner Curio Cabinets Due to Tip-Over and Entrapment Hazards; Sold Exclusively at Havertys (Recall Alert)

NHTSA Critical Jun 18, 2019

ISUZU 2020: STEERING

ISUZU

NHTSA Critical Jun 18, 2019

FORD 2017-2018: EQUIPMENT

FORD

NHTSA Critical Jun 18, 2019

FORD 2017: EXTERIOR LIGHTING:BRAKE LIGHTS

FORD

NHTSA Critical Jun 14, 2019

MASERATI 2017: AIR BAGS

MASERATI

NHTSA Critical Jun 14, 2019

MERCEDES-BENZ 2016-2017: POWER TRAIN:DRIVELINE:DRIVESHAFT

MERCEDES-BENZ

NHTSA Critical Jun 14, 2019

PETERBILT 2010-2020: EXTERIOR LIGHTING:TURN SIGNAL

PETERBILT

CPSC Moderate Jun 13, 2019

American Honda Recalls Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)

American Honda Motor Company Inc., of Torrance, Calif.

NHTSA Critical Jun 13, 2019

JEEP 2019: AIR BAGS

JEEP

NHTSA Critical Jun 13, 2019

JEEP 2014: POWER TRAIN:AUTOMATIC TRANSMISSION

JEEP

FDA Food Moderate Jun 12, 2019

Strawberry Banana Smoothie, 3.1oz, 6 pack, UPC Code 52159-70082

Stonyfield Farm

FDA Food Critical Jun 12, 2019

Bacon Shallot Potato Salad, internal item PLU code 52365, sold as bulk from the full service deli case per costumers order. The salad was packed int…

New Seasons Market LLC

FDA Food Critical Jun 12, 2019

Gia Russa Whole Grain Italian Seasoned Bread Crumbs in 10 Oz Paperboard Canisters

Icco Cheese Co Inc

FDA Food Moderate Jun 12, 2019

10.5 " Flat Edge Pizza Crust, packaged in a box with 40 pieces per box

Value Added Products

FDA Food Moderate Jun 12, 2019

Topnotch Foods Italian Bread Crumbs: 10 lb. Net Wt.. 10 lbs. (4.54 Kg) Item number 10008: Vernon, CA 90058 Correct ingredients: CRUMBS: Enr…

Topnotch Foods Inc

FDA Food Critical Jun 12, 2019

Topnotch Foods Natural Bread Crumbs: 50 lb. Net Wt. 22.68 kg. and 10 lbs. 4.54 Kg. Item number 10021: Vernon, CA Correct Ingredients: Enri…

Topnotch Foods Inc

FDA Food Moderate Jun 12, 2019

Young Ocean brand Seasoned Alaskan Pollock Roe, frozen, wrapped in plastic liner and packed in styrofoam box, and finally packed in cardboard box. N…

Young Ocean, Inc

FDA Food Moderate Jun 12, 2019

Art Cream Gluten Free Cookies & Cream ice cream, one pint. UPC 57897-00803. Products have been manufactured on Shared Equipment that Processes Pean…

Sassy Cow Creamery, LLC

FDA Food Critical Jun 12, 2019

Gia Russa Whole Grain Italian Unseasoned Bread Crumbs in 10 Oz Paperboard Canisters

Icco Cheese Co Inc

FDA Devices Moderate Jun 12, 2019

Thoracentesis Set, RPN C-THS-850, Order # G03286

Cook Inc.

FDA Devices Moderate Jun 12, 2019

Pericardiocentesis Catheter Tray, RPN C-PCSY-850-LHSC-061096, Order # G10030

Cook Inc.

FDA Devices Moderate Jun 12, 2019

IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564451791, 453564451811, 453564467721, 453564467741,…

Philips North America, LLC

FDA Devices Moderate Jun 12, 2019

Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

Stryker Corporation

FDA Devices Moderate Jun 12, 2019

AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero Generator PG (1) Catalog Number:12740000 UPN: H78712740000 (2) Solero Gen…

Angiodynamics Inc. (Navilyst Medical Inc.)

FDA Devices Critical Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV28F

OriGen Biomedical, Inc.

FDA Devices Low Jun 12, 2019

2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Product Usage: The 2008T hemodialysis machine is indicated for a…

Fresenius Medical Care Renal Therapies Group, LLC

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2019 with 2018 →

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 2019