PlainRecalls

2019 Recalls

6,365 recalls · Page 2 of 128

2019 Recall Year Insight

Federal agencies issued 6,365 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 7.58% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 128 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 13 critical, 31 moderate, and 6 lower-severity recalls. The page references 29 distinct recalling firms operating in 5 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), FDA Food (13), FDA Drug (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 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Critical Dec 25, 2019

SLAW COCONUT CITRUS served on the salad bar

Whole Foods Market

FDA Food Critical Dec 25, 2019

CAULIFLOWER BROCCOLI ETHIOPIAN served on the hot bar

Whole Foods Market

FDA Food Critical Dec 25, 2019

Cauliflower Caulilini sold on the salad bar

Whole Foods Market

FDA Food Moderate Dec 25, 2019

Trend Alert Caulilini with Vadouvan Curry served on the salad bar

Whole Foods Market

FDA Food Critical Dec 25, 2019

BROCCOLI GARLIC SUNDRIED TOMATOES and served on the salad bar

Whole Foods Market

FDA Food Moderate Dec 25, 2019

Freshness Guaranteed Croissants in clear plastic 12oz clamshell, 12 clamshells per case, item number 7012

Gold Standard Baking, Inc.

FDA Food Critical Dec 25, 2019

Chicken Cashew sold on the hot bar and in chef's case

Whole Foods Market

FDA Food Critical Dec 25, 2019

Caulilini, Roasted sold on the salad bar

Whole Foods Market

FDA Food Critical Dec 25, 2019

Bulgogi Beef with Vegetables sold on the hot bar

Whole Foods Market

FDA Food Moderate Dec 25, 2019

Hodgson Mill Unbleached All-Purpose White Wheat Flour 5 Lb bags 001042 Best By 10-01-2020 005517 Best By 10-02-2020

Cell-nique Corp dba Living Harvest at Hudson River Foods

FDA Food Critical Dec 25, 2019

SALAD BROCCOLI KALE served on the hot bar

Whole Foods Market

FDA Food Moderate Dec 25, 2019

Salmon Dinner with Lemon Herb for 2 packaged in the store UPC 20451100000

Whole Foods Market

FDA Food Moderate Dec 25, 2019

Vegetable eggroll 2 oz. and 3 oz.

T & R Enterprises USA, Inc.

FDA Drug Low Dec 25, 2019

VCF Vaginal Contraceptive Foam, a) can, 13 applications per can, Net wt. 0.6 oz (17g). NDC 52925-312-14, b) case pack with 36 cans in a nested contai…

Apothecus Pharmaceutical Corp.

FDA Drug Critical Dec 25, 2019

Levetiracetam Oral Solution 100mg/mL, 473 mL (16 fl. oz.) Bottles, Rx Only, Distributed by: Lannett Company, Inc. Philadelphia, PA 19136, NDC 54838-0…

Lannett Company, Inc.

FDA Drug Low Dec 25, 2019

Memantine Hydrochloride Extended-release Capsules, 28mg, packaged in a) 90-count bottles (NDC 68180-249-09 and b) 500-count bottles (NDC 68180-249-02…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Dec 25, 2019

Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99

AuroMedics Pharma LLC

FDA Drug Moderate Dec 25, 2019

Estriol, USP (Micronized) 1 g, 5 g, 25 g, 100 g, 2000 g, 1 kg, containers, Packed by Medisca Inc., Plattsburgh, NY 12901, USA

Medisca, Inc.

FDA Devices Moderate Dec 25, 2019

HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes - Product Usage: An electroco…

Bio-Signal Group Corp.

FDA Devices Moderate Dec 25, 2019

Aestiva 7900, Model Numbers: a) 1006-9300-000 b) 1006-9305-000 c) 1006-9118-000 d) 1006-9112-000 e) 1006-9113-000 f) 1006-9020-000 g) 100…

GE Healthcare, LLC

FDA Devices Moderate Dec 25, 2019

OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Usage: pre-calibrated PSD sensors are intended for …

Angiodynamics, Inc.

FDA Devices Low Dec 25, 2019

Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40, Style 45 Style 10/UDI: NATRE…

Allergan PLC

FDA Devices Moderate Dec 25, 2019

Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J

Arrow International Inc

FDA Devices Moderate Dec 25, 2019

Aespire 7100, Model Numbers: 1. 1009-9000-000-009469 2. 1009-9000-000 3. 1009-9000-000-013913 4. 1009-9000-000-001366 5. 1009-9000-000-009857 …

GE Healthcare, LLC

FDA Devices Moderate Dec 25, 2019

Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130

Arrow International Inc

FDA Devices Moderate Dec 25, 2019

A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054, 3062

Polymer Technology Systems

FDA Devices Moderate Dec 25, 2019

Low Volume Cartridge IFU (SKU CAR-125-B) used with the following devices: 1) NxStage One, Model NX1000-1; 2) NxStage VersiHD Cycler, Model Number…

NxStage Medical, Inc.

FDA Devices Low Dec 25, 2019

Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style LP/UDI: NATRELLE Style 68LP…

Allergan PLC

FDA Devices Moderate Dec 25, 2019

TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.

Tekia, Inc.

FDA Devices Moderate Dec 25, 2019

CVS Health At Home A1C Test Kit, Software Version Revision D, REF Number 3059

Polymer Technology Systems

FDA Devices Moderate Dec 25, 2019

Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Dec 25, 2019

Aestiva 7100, Model Numbers: 1. 1006-9320-000 2. 1006-9321-000 3. 1006-9320-000-001101 4. 1006-9021-000 5. 1006-9012-000 6. 1006-9111-000 7…

GE Healthcare, LLC

FDA Devices Moderate Dec 25, 2019

DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP

DeRoyal Industries Inc

FDA Devices Moderate Dec 25, 2019

OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treat…

Angiodynamics, Inc.

FDA Devices Moderate Dec 25, 2019

Aestiva MRI, Model Numbers: a) 1006-9310-000 b) 1006-9110-000 c) 1006-9023-000 d) 1006-9028-000 e) 1006-9310-000-305077 f) 1006-9310-000-015243…

GE Healthcare, LLC

FDA Devices Moderate Dec 25, 2019

smith&nephew PROFIX Mallet, 750 GRAMS, REF 71512452 - Product Usage: The PROFIX Mallet is a reusable surgical instrument used to tap instruments or i…

Smith & Nephew, Inc.

FDA Devices Moderate Dec 25, 2019

Roche Homocysteine-In vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c system…

Roche Diagnostics Operations, Inc.

FDA Devices Moderate Dec 25, 2019

LIFESTREAM Balloon Expandable Vascular Covered Stent . BARD PERIPHERAL VASCULAR. 6mm X 26mm X 80 Recommended Introducer 6F (2.00mm) NP 8atm (811 kP…

Bard Peripheral Vascular Inc

FDA Devices Moderate Dec 25, 2019

VisuMax Software Version 2.10.13 with activated Software-Module ReLEx (SMILE) option used in conjunction with the VisuMax Femtosecond Laser System fo…

Carl Zeiss Meditec, Inc.

FDA Devices Moderate Dec 25, 2019

A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038, 3057, 3058

Polymer Technology Systems

FDA Devices Moderate Dec 25, 2019

MICRO-PSD HDR, Catalog Number: PSD-HB5N - Product Usage: pre-calibrated PSD sensors are intended for use during cancer treatments to measure photon a…

Angiodynamics, Inc.

FDA Devices Moderate Dec 25, 2019

AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D 105650-001H 105650-001R 105650-001Z 105650-002R 105650-004H 105650-004R 105650…

Boston Scientific Corporation

FDA Devices Low Dec 25, 2019

Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles and Sizes: 7607 SSM, 7608 SSF, 7609 SSX, 7513 SRL, 7514 SRLP, 7515 SRM, 75…

Allergan PLC

FDA Devices Low Dec 25, 2019

QuickTox 5 Panel Drug Screen DipCard

Ameditech Inc

CPSC Moderate Dec 20, 2019

Bosch Thermotechnology Recalls Buderus Boilers Due to Carbon Monoxide Poisoning Hazard

Bosch Thermotechnik GmbH, of Germany

CPSC Moderate Dec 20, 2019

Hallmark Recalls Candles Due to Fire and Laceration Hazards

Hallmark Marketing Company LLC, of Kansas City, Mo.

NHTSA Critical Dec 20, 2019

MERCEDES-BENZ 2002-2011: VISIBILITY:SUN/MOON ROOF ASSEMBLY

MERCEDES-BENZ

NHTSA Critical Dec 20, 2019

PETERBILT 2019: STEERING

PETERBILT

NHTSA Critical Dec 20, 2019

MERCEDES-BENZ 2018: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS

MERCEDES-BENZ

NHTSA Critical Dec 20, 2019

MERCEDES-BENZ 2019: EQUIPMENT:OTHER:LABELS

MERCEDES-BENZ

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2019