PlainRecalls

2019 Recalls

7,396 recalls · Page 96 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 18 critical, 30 moderate, and 2 lower-severity recalls. The page references 21 distinct recalling firms operating in 6 distinct product categories, with 44 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (17), FDA Devices (13), FDA Drug (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 Devices Moderate Jun 5, 2019

Maquet Getinge-T 8029 PRESSURE PIGTAIL 6" Material: 701055995

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 36504 ADULT ECC PACK Material: 701065765

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T 8025 1/4" ECC Pack with RF32 Material:701055142

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Fenestrated Tap Adapter (REF# 5001-90011) Product Usage: The K2M Fenestrated Tap System is intended for use as a standalone biopsy tool to remove…

K2M, Inc

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-T 44201 MAYO PULMONARY PACK Material: 701064834

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge- BEQ-TOP 32100 Adult Custom Pack Material:701054438R01

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 30300 Material:701052623

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-TOP 30907 ECC PUMP PACK Material: 701065770

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 20705 SMALL PATIENT 1/4 Material: 701053486R01

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BO-TOP 35503 SGD PACK Material: 701067668

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T 4903 Mercy Med w/o Oxy Material:701066664

Maquet Cardiovascular, LLC

FDA Devices Moderate Jun 5, 2019

RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

Teleflex Medical

FDA Devices Moderate Jun 5, 2019

Maquet Getinge-BEQ-T 52301 ¿ Sash & Accessory Pack Material: 709000266

Maquet Cardiovascular, LLC

CPSC Moderate Jun 5, 2019

Apple Recalls Three-Prong Wall Plug Adapters Included in World Travel Adapter Kit Due to Risk of Electric Shock

NHTSA Critical Jun 5, 2019

AUDI 2018-2019: WHEELS:HUB

AUDI

NHTSA Critical Jun 5, 2019

AUDI 2019: SEATS

AUDI

NHTSA Critical Jun 5, 2019

FORD 2018: EQUIPMENT

FORD

CPSC Moderate Jun 4, 2019

Generation Brands Recalls Glass Pendant Light Fixtures Due to Risk of Injury

Guangzhou Xiongyi Precision Metalworking Co., Ltd., of China

CPSC Moderate Jun 4, 2019

Polaris Recalls Recreational Off Highway Vehicles Due to Crash Hazard (Recall Alert)

Polaris Industries Inc., of Medina, Minn.

CPSC Moderate Jun 4, 2019

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

Polaris Industries Inc., of Medina, Minn.

NHTSA Critical Jun 4, 2019

HONDA 2018-2019: POWER TRAIN:MANUAL TRANSMISSION

HONDA

NHTSA Critical Jun 4, 2019

FERRARI 2016-2018: AIR BAGS: AIR BAG/RESTRAINT CONTROL MODULE

FERRARI

CPSC Moderate May 30, 2019

Excel Industries Recalls Zero-Turn Mowers Due to Fire Hazard (Recall Alert)

Excel Industries Inc., of Hesston, Kans.

NHTSA Critical May 30, 2019

MAZDA 2018: ELECTRICAL SYSTEM:WIRING

MAZDA

FDA Food Critical May 29, 2019

Ham and Cheddar Sandwich 7.75 OZ.

Great American Marketing Company

FDA Food Critical May 29, 2019

Life Rising Holder-W Holder Warmer capsules, 54 count bottle

Life Rising Corporation

FDA Food Moderate May 29, 2019

Trader Joe s Vegetable Melange In Seasoned Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0033 7038

Ardo N.V.

FDA Food Critical May 29, 2019

Deli Cut Turkey Sandwich 5.5 OZ.

Great American Marketing Company

FDA Food Critical May 29, 2019

HoliCare Metabolism Cleansing (MET-CLS) tablets, 60 count bottle

Life Rising Corporation

FDA Food Moderate May 29, 2019

Life Rising NECK-ND Neck Clear capsules, 54 count bottle

Life Rising Corporation

FDA Food Critical May 29, 2019

Turkey Pepper Jack 6" Sub Sandwich with Jalapeno Ranch Dressing 5.5 OZ.

Great American Marketing Company

FDA Food Critical May 29, 2019

Deli Cut Ham and American Sandwich 5.5 OZ.

Great American Marketing Company

FDA Food Moderate May 29, 2019

Trader Joe s Fire Roasted Vegetables With Balsamic Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0077 5175

Ardo N.V.

FDA Food Critical May 29, 2019

Deshi Golden Raisin, packaged in 3.5 oz, 7 oz. and 14 oz. clear plastic

DESHI DISTRIBUTORS, LLC

FDA Food Low May 29, 2019

Goji Powder (aka Wolfberry Powder)

Xi'an Yuensun Biological Technology Co., Ltd.

FDA Food Critical May 29, 2019

Jalapeno Pimento Cheese Sandwich 4.5 OZ.

Great American Marketing Company

FDA Food Critical May 29, 2019

Mecox Bay Dairy Sunrise Raw Milk Cheese in plastic wrap code L 2148 Size Range between .25 lb to 3 lb portions of a 3 lb wheel.

Mecox Bay Dairy

FDA Food Critical May 29, 2019

Turkey and Swiss Sandwich 8.0 OZ.

Great American Marketing Company

FDA Food Low May 29, 2019

Haikui Abalone in Brown Sauce 3 oz pouch bag,UPC Code: 719926149198

Haiku(Us) Mr Ocean Seafood Corp.

FDA Food Critical May 29, 2019

Chicken Salad Sandwich 4.5 OZ.

Great American Marketing Company

FDA Food Critical May 29, 2019

Italian 6" Sub with HAM, COTTO SALAMI, PEPPERONI & CHEESE: 5.5 OZ

Great American Marketing Company

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated

Golden State Medical Supply Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 100 mg 90 film coated tablets Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 …

Heritage Pharmaceuticals, Inc.

FDA Drug Moderate May 29, 2019

Amitiza (lubiprostone) capsules, 8 mcg, 60-count bottle, Rx only, Manufactured by: Sucampo Pharma Americas, LLC, NDC 64764-080-60

MALLINCKRODT PHARMACEUTICALS

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 25 mg 1000 count bottle NDC 60429-316-10 Rx only GSMS Incorporated

Golden State Medical Supply Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 50 mg 90 film coated tablets Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 …

Heritage Pharmaceuticals, Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 100 mg 1000 count bottle NDC 60429-318-10 Rx only GSMS Incorporated

Golden State Medical Supply Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 25 mg 90 film coated tablets Rx Only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107…

Heritage Pharmaceuticals, Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 100 mg 90 count bottle NDC 60429-318-90 Rx only GSMS Incorporated

Golden State Medical Supply Inc.

FDA Drug Moderate May 29, 2019

Losartan Potassium Tablets USP 100 mg 1000 film coated tablets Rx only Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102,…

Heritage Pharmaceuticals, Inc.

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