PlainRecalls

2024 Recalls

4,937 recalls · Page 91 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 4 critical, 46 moderate, and 0 lower-severity recalls. The page references 15 distinct recalling firms operating in 5 distinct product categories, with 27 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (43), NHTSA (4), CPSC (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 Devices Moderate Feb 7, 2024

Terragene Bionova PCD (PCD222-C)

TERRAGENE S.A.

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #9 -Intended for knee replacement Part Number: 73-0910

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

DUR PCA MTK REV INS LFT Intended for knee replacement Product Number: 6728-2-611

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210

FX SHOULDER

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general & plastic surgery, labeled as: a) BRACHY THERAPY PROCEDURE PAC, kit number AGBR90E; b) BRA…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

MB215R - MILLS DUROGRIP TC Micro Needle Holder, straight, 8:, (203 mm), "TC MILLS NDLE HOLDRRND HNDLSTR203MM"

Aesculap Inc

FDA Devices Moderate Feb 7, 2024

TIBIAL BEARING INSERT SERIES P-S I ASSY Intended for knee replacement Product Number: 7291-0324

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-416

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, gastroenterological & urological, labeled as: a) LAP KIDNEY MODULE, kit number AGKD50L; b) ROBOTIC…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 ye…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Product Number: 6742-1-413

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years)…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

DUR PCA MTK REV INS RT Intended for knee replacement Product Number: 6728-2-711

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 7, 2024

HOWMEDICA OSTEONICS TRIDENT 0 deg POLY INSERT Intended for knee replacement Part Number: 620-00-28J

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Achieva XR. Model (REF) Numbers 781153, 781253.

Philips North America

FDA Devices Moderate Feb 7, 2024

P7 28MM 10 DEGREE +4MM INSERT Intended for knee replacement Part Number: 6302-6-107

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

ENDOPATH ECHELON 45mm RELOADS WITH GRIPPING SURFACE TECHNOLOGY (GST), ECHELON Endopath Stapler, Endoscopic Linear Cutter Reload (+Gripping Surface …

Ethicon Endo-Surgery Inc

FDA Devices Moderate Feb 7, 2024

RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-931

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SERIES II TIBIAL BEAR INSERT-Intended for knee replacement Part Number: 3052-0524

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7521

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

LEFT LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part Number: 6637-0-228

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- Intended for knee replacement Part Number: 72-15-0324

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

LEFT X-LARGE-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-328

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

P7 32MM 1O DEGREE +4MM INSERT Intended for knee replacement Part Number: 6302-6-307

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Mo…

Olympus Corporation of the Americas

FDA Devices Moderate Feb 7, 2024

MEDLINE ADULT BLOOD CULTURE KIT, Reorder Number DYNDH1694A

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Feb 7, 2024

NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL

THOR Photomedicine Ltd

FDA Devices Moderate Feb 7, 2024

MB362R - JACOBSON DUROGRIP TC Micro Needle Holder, straight, 8 3/4", (220 mm), "TC JACOBSON NDL HLD STR JAW 220MM";

Aesculap Inc

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) Baby PICC Kit, kit number UIBP90J; b) Baby PICC Kit, kit numb…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #11 -Intended for knee replacement Part Number: 73-2110

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Achieva 1.5T Initial system. Model (REF) Numbers 781178.

Philips North America

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) LOWER PELVIC PACK, kit number AGLP52L; b) OB/GYN D…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

DURATION PLASTIC PATELLA-DURACON Intended for knee replacement Product Number: 6642-2-200

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT-Intended for knee replacement Part Number:72-4-7512

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7524

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Terragene Integron IT26-C Terragene Integron IT26-C with extender Benco Dental Chemical Integrator [5726-583] Tuttnauer (WTL198-0082) Ter…

TERRAGENE S.A.

FDA Devices Moderate Feb 7, 2024

RGT.LARGE-PCA MOD.REV.- DUR.REV.INSERT Intended for knee replacement Product Number: 6637-0-928

Howmedica Osteonics Corp.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, Obstetrical & Gynecological use, labeled as: a) C-SECTION PACK, kit number FDCS01AA; b) C-SECTION …

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, cardiac, labeled as: a) HEART CATHETERIZATION TRAY, kit number JRHC45G; b) TAVR PACK, kit number L…

American Contract Systems, Inc.

FDA Devices Moderate Feb 7, 2024

Custom procedural convenience kits and trays, general hospital use, labeled as: a) IR NEURO PACK, kit number AGNE20J; b) ADULT CRANIOTOMY PACK, …

American Contract Systems, Inc.

NHTSA Critical Feb 7, 2024

KIA 2024: ENGINE AND ENGINE COOLING:ENGINE:HARD PARTS INTERNAL/MECHANICAL

KIA

NHTSA Critical Feb 7, 2024

LUCID 2022-2024: FORWARD COLLISION AVOIDANCE: ADAPTIVE CRUISE CONTROL:SOFTWARE

LUCID

NHTSA Critical Feb 2, 2024

NISSAN 2018-2022: BACK OVER PREVENTION: SENSING SYSTEM: CAMERA

NISSAN

NHTSA Critical Feb 2, 2024

MERCEDES-BENZ 2019-2022: EXTERIOR LIGHTING:HEADLIGHTS

MERCEDES-BENZ

CPSC Moderate Feb 1, 2024

BISSELL Recalls Multi Reach Hand and Floor Vacuum Cleaners Due to Fire Hazard

CPSC Moderate Feb 1, 2024

Box Components Recalls BMX Race Bicycle Stems Due to Fall Hazard

The Cycle Group, Dba Box Components, from Anaheim, California

CPSC Moderate Feb 1, 2024

Children's Nightgowns Recalled Due to Fire and Burn Hazard; Violation of Federal Flammability Regulations; Imported by Shenzhen Weite Information Tec…

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