PlainRecalls

2019 Recalls

7,611 federal recalls indexed for 2019 · Page 78 of 153

2019 Recall Year Insight

Federal agencies issued 7,611 product recalls indexed by PlainRecalls in calendar year 2019. That represents about 7.29% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 20.9 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 153 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 10 critical, 40 moderate, and 0 lower-severity recalls. The page references 28 distinct recalling firms operating in 7 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (31), CPSC (8), NHTSA (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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

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FDA Devices Moderate Jul 31, 2019

VITALE Silicon Foam Dressings 4"x4" Cat. No. 20144

CellEra LLC
FDA Devices Moderate Jul 31, 2019

Zyno Medical Administration Set -105"ADMIN SET 20DP W/FILTER 2YSITES CLMP- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code: B2-70072-F

Zyno Medical LLC
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 15 G x 1-1/2" (1.829 mm x 3.8 cm) Item code: 8881202314

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.

Zevex Incorporated (dba MOOG Medical Devices Group)
FDA Devices Moderate Jul 31, 2019

PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System is indicated in patients where cardiovascular and circulatory volume status monitoring is necessary. If a patient s biometric data are entered, the PulsioFlex Monitor presents the derived parameters indexed. ¿ -With the PiCCO Module cardiac output is determined both continuously through pulse contour analysis and intermittently through thermodilution technique. Both are used

GETINGE US SALES LLC
FDA Devices Moderate Jul 31, 2019

BrightView X , Model Number 882478

Philips Medical Systems (Cleveland) Inc
FDA Devices Moderate Jul 31, 2019

AXIOM Artis BA, Model Number 5904656

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

RX Daytona, Model Nos. RX4040 and RX4041

Randox Laboratories, Limited
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 22G x 3/4", Product Code 100279

Terumo Medical Corporation
FDA Devices Moderate Jul 31, 2019

Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

Zyno Medical Administration Set -105"ADMIN SET 20DP, W/2 Y SITE, CVCLMPS- For Use with Zyno Medical Infusion pumps or Gravity Feed Product Code:B2-70072

Zyno Medical LLC
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 18 G x 1-1/2" Item code: 8881200078

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

Terumo Sur-vet Needle, 25G x 5/8", Product Code 100220

Terumo Medical Corporation
FDA Devices Moderate Jul 31, 2019

U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract dysfunctions

LABORIE MEDICAL TECHNOLOGIES, CORP
FDA Devices Moderate Jul 31, 2019

AXIOM Artis BC, Model Number 5904649

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

RX Imola, Model Nos. RX4900

Randox Laboratories, Limited
FDA Devices Moderate Jul 31, 2019

AXIOM Artis FC, Model Number 5904433

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light scattering, measured by reading turbidity at 700 nm, which correlates with the concentration of transferrin in the sample.

Abbott Laboratories, Inc
FDA Devices Moderate Jul 31, 2019

Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

AXIOM Artis dBC, Model Number 5917054

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

AXIOM Artis MP, Model Number 5904466

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

Nimbus Administration Set, REF HS-004, UDI # 00817170020031 Product Usage: Administer fluids/medication from a container to a patient through a needle or a catheter.

InfuTronix LLC
FDA Devices Moderate Jul 31, 2019

AXIOM Artis TC, Model Number 7728350

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.

Medical Intelligence Medizintechnik Gmbh
FDA Devices Moderate Jul 31, 2019

C3 is an in vitro diagnostic assay for the quantitative determination of C3 in human serum or plasma. Antibodies to C3 combine with C3 in the sample to form insoluble immune complexes. The immune complexes cause an increase in light scattering (turbidity). The resulting increase in sample turbidity, measured at 604 nm, is directly proportional to the concentration of C3 in the sample.

Abbott Laboratories, Inc
FDA Devices Moderate Jul 31, 2019

Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654

Cardinal Health 200, LLC
FDA Devices Moderate Jul 31, 2019

The,K -ASSAY HP assay is intended for the quantitative determination of human haptoglobin by immunoturbidimetric assay. The antiserum used in the kit was produced against purified human haptoglobin. The haptoglobin antibody interacts with the haptoglobin in the serum forming immune complexes . The immune complexes cause an increase in light scattering which correlates with the concentration of haptoglobin.

Abbott Laboratories, Inc
FDA Devices Moderate Jul 31, 2019

AXIOM Artis dFC, Model Number 7412807

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

Artis zee biplane MN, Model Number 10094143

Siemens Medical Solutions USA, Inc
FDA Devices Moderate Jul 31, 2019

Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355

Cardinal Health 200, LLC
CPSC No agency class Jul 31, 2019

Dorel Juvenile Group USA Recalls Inclined Sleepers Due to Safety Concerns About Inclined Sleep Products

Dorel China, of China
CPSC No agency class Jul 31, 2019

London Bridge Recalls Sock and Wrist Rattle Sets Due to Choking Hazard
NHTSA No agency class Jul 31, 2019

BMW 2018-2019: SEATS

BMW
USDA FSIS Moderate Jul 31, 2019

Conagra Brands, Inc. Recalls Canned Beef Products Due to Possible Processing Defect

Hometown Food Company
CPSC No agency class Jul 30, 2019

Tristar Products Recalls Magnetic Trivets Due to Magnet Ingestion Hazard (Recall Alert)

Tianxi Holding Group Co Ltd., of China
NHTSA No agency class Jul 29, 2019

MAZDA 2019: VISIBILITY:GLASS, SIDE/REAR

MAZDA
USDA FSIS Critical Jul 27, 2019

Premium Foods USA, Inc., Recalls Siluriformes Products Produced Without Benefit of Import Inspection
CPSC No agency class Jul 26, 2019

Spansive Recalls Wireless Phone Chargers Due To Burn Hazard (Recall Alert)
NHTSA No agency class Jul 26, 2019

RAM 2019: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

RAM
USDA FSIS Critical Jul 26, 2019

Kent Quality Foods, Inc. Recalls Ready-To-Eat Sausage Products due to Possible Foreign Matter Contamination

Kent Quality Foods Inc.
CPSC No agency class Jul 25, 2019

Britax Recalls Modified Thru-Bolt Axles for Use with BOB Jogging Strollers Distributed Through the BOB Information Campaign Due to Fall and Injury Hazards (Recall Alert)

Britax Child Safety Inc., of Fort Mill, S.C.
CPSC No agency class Jul 25, 2019

Cycling Sports Group Recalls Cannondale CAADX Cyclocross Bicycles Due to Fall and Serious Injury Hazard; One Fatality Reported

Cycling Sports Group Inc., of Wilton, Conn.
CPSC No agency class Jul 25, 2019

H&M Recalls Children's Pajamas Due to Violation of Federal Flammability Standard
CPSC No agency class Jul 25, 2019

Stokke Recalls Infant Steps Bouncers Due to Fall Hazard

DPI BV, of Netherlands
NHTSA No agency class Jul 25, 2019

TOYOTA 2012-2018: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS

TOYOTA
NHTSA No agency class Jul 25, 2019

ALFA ROMEO 2018-2019: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

ALFA ROMEO
USDA FSIS Critical Jul 25, 2019

Home Market Foods, Inc. Recalls Frozen Ready-To-Eat Beef and Pork Meatball Products due to Misbranding and Undeclared Allergens

Home Market Foods, Inc.
FDA Food Critical Jul 24, 2019

Pure Ground Ingredients Organic Fennel Seed, Ground 35 lb. bags Item # FENO-GR Processed and Packaged by: Pure Ground Ingredients 2535 Business Parkway Minden, NV 89423

Pure Ground Ingredients
FDA Food Critical Jul 24, 2019

Gold Medal Flour Mt Bulk Product Code 805046

ADM - CHICAGO

Nearby Recall Years

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

2017 2018 2020 2021 2022

Compare 2019 with 2018 →

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 2019

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 2019 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.