2019 Recalls

Reviewed by PlainRecalls Editorial, Product Recalls Editorial Team

7,396 recalls · Page 81 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 5 critical, 43 moderate, and 2 lower-severity recalls. The page references 21 distinct recalling firms operating in 6 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), FDA Food (13), CPSC (8), 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.

2019 Recalls

2019 Recall Year Insight

Powerheart¿ G5 Automatic AED

EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid…

SOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is inten…

Siemens Artis zee ceiling -Interventional Fluoroscopic X-Ray System Model Number: 10094137

Siemens Artis Q.zen ceiling-Interventional Fluoroscopic X-Ray System Model Number: 10848354

VITROS 250 Chemistry System, Product Code 8132086, (UDI # 10758750004409) Product Usage: Performs discrete clinical tests on serum, urine, and …

Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem im…

VITROS 250 Chemistry System Refurbished, Product Code 6801759, (UDI # 10758750001330) Product Usage: Performs discrete clinical tests on serum, …

SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is inte…

Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model Number: 10848282

SOMATOM go.Up, Model No. 11061628 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is i…

cobas p 501 post-analytical units, Part Number 05158494001. For diagnostic sample storage and retrieval.

Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item necessary to perform one vitr…

VITROS 250AT Chemistry System, Product Code 1758143, (UDI # 10758750000036) Product Usage: Performs discrete clinical tests on serum, urine, and…

REVACLEAR 300 Dialyzer, Product Code 114745L Revaclear 300 and Revaclear 400 dialyzers are indicated for treatment of chronic and acute renal fai…

Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Model Number: 10848353

First Step Draco Pad, Product Number EP-4D

Atellica CH Creatine Kinase (CK_L) Reagent, Product Code 11097640, UDI Number: 00630414006642 - Product Usage: The ADVIA¿ Chemistry Creatine Kinase (…

Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Model Number: 10849000

Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic review, analysis, annotation, distrib…

cobas p 701 post-analytical units, Part Number 05349966001. For diagnostic sample storage and retrieval.

Siemens Artis Q.zen biplane-Interventional Fluoroscopic X-Ray System Model Number: 10848355

Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z

SOMATOM go.All, Model No. 11061638 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This computed tomography system is …

CLEO Patient Monitor /Tranquility VS Patient Monitor

Siemens Artis zeego--Interventional Fluoroscopic X-Ray System Model Number: 10280959

Bose Recalls EdgeMax® and FreeSpace® Loudspeakers Due to Injury Hazard (Recall Alert)

Custom Molded Products Recalls Valve Caps Sold With Hot Tubs/Swim Spas Due to Impact Hazard

Everbilt Door Pulls Recalled Due to Laceration Hazard; Sold Exclusively at Home Depot; Made by Wellsco International Group

Office Depot Recalls Desks Due To Shock Hazard (Recall Alert)

Universal Security Instruments Recalls to Inspect Smoke Alarms Due to Risk of Failure to Alert Consumers to a Fire

Winco Fireworks Recalls Black Cat "Cat Mobiles" Due to Explosion, Burn and Projectile Hazards

FORD 2019: SEAT BELTS

Swaddle Bee Recalls Children's Security Blankets Due to Choking Hazard (Recall Alert)

Disney Recalls the Forky 11" Plush Toy Due to Choking Hazard

FORD 2012-2017: FUEL SYSTEM, GASOLINE:STORAGE

MAZDA 2019: SEATS:FRONT ASSEMBLY:HEAD RESTRAINT

Double Chocolate Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Blueberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Banana Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Triple Play Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Neapolitan Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Tiramisu Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Dreamsicle Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Cream Cheese Brownies in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Snickers Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Chocolate Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Chocolate Raspberry Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117

Karawan Tahini, Net Weight: 3Kg (105.822 oz)

Spicy Shrimp Tempura Crunch Roll, Mai brand, packed in container with clear plastic lid,net wt. 9.1 oz., UPC 8 12824 01526 5. The label is read in…

Nearby Recall Years

Data Sources