PlainRecalls

2024 Recalls

4,937 recalls · Page 90 of 99

2024 Recall Year Insight

Federal agencies issued 4,937 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 5.88% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 13.5 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 99 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 3 critical, 47 moderate, and 0 lower-severity recalls. The page references 16 distinct recalling firms operating in 3 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), FDA Drug (3), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Feb 7, 2024

Cefixime for Oral Suspension 100mg/5mL, 50 mL bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Feb 7, 2024

Rifampin Capsules USP 300mg, 30-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufa…

Lupin Pharmaceuticals Inc.

FDA Drug Moderate Feb 7, 2024

OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl alcohol 6.0% Antibacterial, Manufactured by: Den-Mat Holdings, LLC, Lompoc, C…

Den-Mat Holdings, LLC

FDA Devices Moderate Feb 7, 2024

Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement Part Number: 72-16-0910

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product Number: 6637-4-031

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Surgilon Braided Nylon sutures: 88861919-31 SURGILON* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON* 3-0 BLK 7X75CMPCT 88861919-51 SURGILON* 2-0 BLK 7X…

Covidien LP

FDA Devices Moderate Feb 7, 2024

PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-411

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-0110

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years) M…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

Intera 1.5T Achieva Nova. Model (REF) Numbers 781172.

Philips North America

FDA Devices Moderate Feb 7, 2024

LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years)…

Olympus Corporation of the Americas

FDA Devices Critical Feb 7, 2024

smiths medical Medfusion Model 3500 Syringe pump

Smiths Medical ASD Inc.

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 7, 2024

Philips Azurion system, Interventional fluoroscopic x-ray system. System Product Name - Model Numbers Azurion 3M12 -722063, 722221; Azurion 3M15 -…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-2910

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

AtriCure, Inc.

FDA Devices Moderate Feb 7, 2024

GE Voluson IC9-RS intracavitary probes, Model Number J48691PJ, Diagnostic ultrasound imaging and fluid flow analysis

GE HEALTHCARE AUSTRIA GMBH & CO

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-2710

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model: BD…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

Procedural convenience kits and trays, cardiac, labeled as: a) EP LAB BI V IMPLANT PACK, kit number AGBI64J; b) LAB DEVICE IMPLANT, kit number A…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, ear, nose & throat, labeled as: a) T AND A PACK AGH ASC, kit number AGTA48J; b) OPSC EAR PACK, kit…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

Cortera Spinal Fixation System, REF: 150100-85050. Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length.

XTANT Medical Holdings, Inc

FDA Devices Moderate Feb 7, 2024

DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement Product Number: 6642-1-911

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LavH, kit number BBLV21C; b) LAP HYST 247540, ki…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 7, 2024

SmartPath to dStream for XR and 3.0T. Model (REF) Numbers 781270, 782113, 782129.

Philips North America

FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028

Howmedica Osteonics Corp.

FDA Devices Critical Feb 7, 2024

smiths medical Medfusion Model 4000 syringe pump

Smiths Medical ASD Inc.

FDA Devices Moderate Feb 7, 2024

Volar Bearing Plate. REF: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N, VBEAR-3-7S…

TriMed Inc.

FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, cardiac, labeled as: a) CENTRAL LINE INSERTION PACK, kit number LLCE52; b) Adult Central Line Inse…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 7, 2024

LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-028

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-609

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). …

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

AtriCure, Inc.

FDA Devices Moderate Feb 7, 2024

Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105.

Philips North America

FDA Devices Moderate Feb 7, 2024

Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25

Vortex Surgical Inc.

FDA Devices Moderate Feb 7, 2024

HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-32J

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Fixed Wire Balloon 18-19-20. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model:…

Olympus Corporation of the Americas

FDA Devices Critical Feb 7, 2024

EVair 03 (Jun-air) air compressor, model numbers: 1609000 and 1609002

Datex-Ohmeda, Inc.

FDA Devices Moderate Feb 7, 2024

Achieva 1.5T. Model (REF) Numbers 781196, 781343, 781296.

Philips North America

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #7 -Intended for knee replacement Part Number: 73-0710

Howmedica Osteonics Corp.

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: CPSC + NHTSA — consumer product and vehicle recall feeds for 2024