PlainRecalls

2024 Recall Year Insight

Federal agencies issued 6,264 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 6.00% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 17.2 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 126 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 2024.

On this page of 50 records, severity classification shows 4 critical, 46 moderate, and 0 lower-severity recalls. The page references 13 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 2024 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.

FDA Devices Critical Jul 17, 2024

BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)

Synergetics Inc

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE -Procedure Kit Catalog Number: QPTK95A

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE, ST LUKES Catalog Number: LMTK17AP

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

ARTHRO KNEE BEACHES PACK BHS- Procedure tray Catalog Number: BPKB46B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

HAND WRIST FOREARM-LF Procedure tray Catalog Number: CCHD17B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

AHAR50K STANDARD ARTHROSCOPY PACK - 291852. Procedure tray Catalog Number: AHAR50K

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 247546 - Procedure tray Catalog Number: BFTK01AA

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.

Preat Corp

FDA Devices Moderate Jul 17, 2024

CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AG

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo Surgical Lights); e) 4068310 (Ceiling Trio Surgical Lights); f) 4068410 (Ceiling Quad Surgical Lights)

Baxter Healthcare Corporation

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE -Procedure Kit Catalog Number: QPTK95B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical Lights)

Baxter Healthcare Corporation

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 297835 -Procedure Kit Catalog Number: RGTK10L

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

BPKN15C KNEE BASIN PACK BHS- Procedure tray Catalog Number: BPKN15C

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22U

American Contract Systems Inc

FDA Devices Critical Jul 17, 2024

BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)

Synergetics Inc

FDA Devices Moderate Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic ultrasound system.

Echonous Inc

FDA Devices Critical Jul 17, 2024

BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eye)

Synergetics Inc

FDA Devices Moderate Jul 17, 2024

190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Jul 17, 2024

ARTHO KNEE BAPTIST SOUTH PACK Procedure tray Catalog Number: BPKA49B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

ACL PACK - 206039-Procedure Kit Catalog Number: UDAC66AA

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev A

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE-Procedure Kit Catalog Number: SMTK21C

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

Decompression Table Model E9011. This device applies cervical and/or lumbar decompression with practitioner definable target treatment location, treatment pounds, and patterns of treatment.

Pivotal Health Solutions, Inc.

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

MAJOR KNEE - 302497- Procedure tray Catalog Number: ASKN23B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

Pink Luminous Breast, Breast transilluminator

Silkprousa LLC

FDA Devices Moderate Jul 17, 2024

ORIF HIP - IM RODDING FEMUR-Procedure Kit Catalog Number: UTHP44S

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

Synergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic injections Model/Catalog Number: 18069 Product Description:

MICROspecialties, Inc.

FDA Devices Moderate Jul 17, 2024

Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061

MICROspecialties, Inc.

FDA Devices Moderate Jul 17, 2024

Presource kits and trays, labeled as: 1) Cardiac Catheterization Kit, Catalog Number SAN69CCKRB; 2) Cardiac Catheterization Kit, Catalog Number SAN73CCV10; 3) Cardiac Catheterization Kit, Catalog Number SAN73CCV11; 4) Cardiac Catheterization Kit, Catalog Number SAN73CCV12; 5) Cardiac Catheterization Kit, Catalog Number SAN73CCV13; 6) Cardiac Catheterization Kit, Catalog Number SAN73CCV14; 8) Cardiac Catheterization Kit, Catalog Number SAN73CCVD8; 9) Cardiac Catheterization Kit,

Cardinal Health 200, LLC

FDA Devices Moderate Jul 17, 2024

CUSTOM KNEE - 206061-Procedure Kit Catalog Number: UDKN68AE

American Contract Systems Inc

FDA Devices Critical Jul 17, 2024

BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)

Synergetics Inc

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE - 297835-Procedure Kit Catalog Number: RGTK10K

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

FOOT ANKLE-LF Procedure tray Catalog Number:CCFA51B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part, Model Number: F40015481 Rev A

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Jul 17, 2024

Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W

MICROspecialties, Inc.

FDA Devices Moderate Jul 17, 2024

TOTAL KNEE-Procedure Kit Catalog Number: SFTK54B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

LOWER EXTREMITY - 247542- Procedure tray Catalog Number: BFLE56X

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

Presource kits and trays, labeled as: 1) ANGIOGRAPHY PACK, Catalog Number SAN13BS605; 2) ANGIOGRAPHY PACK, Catalog Number SAN13BS606; 3) ANGIOGRAPHY PACK, Catalog Number SAN13BS607; 4) ANGIOGRAPHY PACK, Catalog Number SAN13BS608; 5) ANGIOGRAPHY PACK, Catalog Number SAN13BS609; 6) STERILE ANGIOGRAPHY PACK, Catalog Number SAN13BS60K; 7) ANGIOGRAPHY PACK, Catalog Number SAN13BS60L; 8) ANGIOGRAPHY PACK, Catalog Number SAN13BS60M; 9) ANGIOGRAPHY PACK, Catalog Number SAN13BS60N; 10) ANGIOGR

Cardinal Health 200, LLC

FDA Devices Moderate Jul 17, 2024

Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060

MICROspecialties, Inc.

FDA Devices Moderate Jul 17, 2024

RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A

Fresenius Medical Care Holdings, Inc.

FDA Devices Moderate Jul 17, 2024

ARTHROSCOPY PACK-Procedure Kit Catalog Number: TNAR22V

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

ACL, ST LUKES METHODIST 1CS Catalog Number: LMAC10AA

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I

American Contract Systems Inc

FDA Devices Moderate Jul 17, 2024

ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA). Model/Catalog Number: G5S-00A G5S-00A-TSO G5S-00C G5S-01A G5S-02A G5S-02C G5S-02-L G5S-04A G5S-05A G5S-05C G5S-06A G5S-06C G5S-08A G5S-08C G5S-10A G5S-10C G5S-11A G5S-11C G5S-12C G5S-13A G5S-14A G5S-15A G5S-17A G5S-17C G5S-19A G5S-

Zoll Medical Corporation

FDA Devices Moderate Jul 17, 2024

The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches. The harvesting tool has two curved jaws. One of the jaws contains the heating elements for branch cutting and cauterization and spot cautery. An area near the tip of the convex side of the jaw is use

Maquet Cardiovascular, LLC

FDA Devices Moderate Jul 17, 2024

GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA

GE Vingmed Ultrasound As

FDA Devices Moderate Jul 17, 2024

KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A

American Contract Systems Inc

Nearby Recall Years

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

Compare 2024 with 2023 →

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 2024

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 2024 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.