PlainRecalls

2024 Recalls

6,210 recalls · Page 84 of 125

2024 Recall Year Insight

Federal agencies issued 6,210 product recalls indexed by PlainRecalls in calendar year 2024. That represents about 6.11% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 17.0 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 125 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 10 critical, 40 moderate, and 0 lower-severity recalls. The page references 25 distinct recalling firms operating in 4 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (45), NHTSA (3), FDA Drug (2), 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 May 1, 2024

minolira (minocycline hydrochloride) extended-release tablets, 105mg 30-count Bottle, Rx Only, Mfg by: Dr Reddy's Laboratories Limited, INDIA, Manufa…

EPI Health, LLC

FDA Drug Critical May 1, 2024

GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.

Pyramids Wholesale Inc.

FDA Devices Critical May 1, 2024

Route 92 Medical, 070 Access System, REF 1004, Rxonly , Sterile EO. Used for introduction of interventional devices into the neurovasculature.

ROUTE 92 MEDICAL INC

FDA Devices Critical May 1, 2024

Route 92 Medical, Tenzing 7 Delivery Catheter, REF 1005, Rx Only, Sterile EO. Used for introduction of interventional devices into the neurovasculatu…

ROUTE 92 MEDICAL INC

FDA Devices Moderate May 1, 2024

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery

Baxter Healthcare Corporation

FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-58F

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-48D

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

Vanguard Knee System AS Tibial Bearing / DCM ArCom, 12 MM X 75 MM; Model Number 189082. The product is placed into a foil pouch with protective packa…

Biomet, Inc.

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-66H

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number: EG-121 Software Version: N/A Product Description: These bottles are sol…

Electro Medical Systems SA

FDA Devices Moderate May 1, 2024

ACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA10G

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate May 1, 2024

Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number: EG-111 Software Version: N/A Product Description: These bottles are s…

Electro Medical Systems SA

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-52E

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

IBA Proton Therapy System - PROTEUS 235, PTS-10 versions, PTS-11 versions, and PTS-12 versions.

Ion Beam Applications S.A.

FDA Devices Moderate May 1, 2024

48" Lead Wires, Replacement Part Number: 1067724-4

EBI, LLC

FDA Devices Moderate May 1, 2024

NexGen CR-Flex Femoral Component, Size E and Size E Minus (E-). Component of the NexGen CR-Flex Porous Femur System.

Zimmer, Inc.

FDA Devices Critical May 1, 2024

Route 92 Medical, Full Length 070 Reperfusion System, REF: 7001, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovas…

ROUTE 92 MEDICAL INC

FDA Devices Moderate May 1, 2024

Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm) x 19 cm (Symmetrical Tip, Heparin Coating, Silver Ion Sleeve and Tal VenaTr…

Covidien LP

FDA Devices Moderate May 1, 2024

LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the LightStrike Germ-Zapping Robots…

XENEX Disinfection Services Inc.

FDA Devices Moderate May 1, 2024

Mariner RDX Polyaxial Head, REF: MX1-000020; Mariner RDX Extended Polyaxial Head, REF: MX1-000030; Mariner RDX Deformity Head, REF: MX1-000040; Ma…

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate May 1, 2024

Mariner RDX MIS Polyaxial Head, REF: MX1-001010, part of Mariner RDX MIS Alpha Instruments and Implants, REF: AMRDXMIS, which are pedicle screw syste…

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-64H

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)

LEICA BIOSYSTEMS NUSSLOCH GMBH

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-50D

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

Alinity m System, Part Number: 08N53-002

Abbott Molecular, Inc.

FDA Devices Moderate May 1, 2024

Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for the treatment of an established nonunion acquired secondary to trauma, …

EBI, LLC

FDA Devices Critical May 1, 2024

VITEK 2 - AST Test kits (in vitro diagnostic test cards for antimicrobial susceptibility): a) AST-N334, REF 418984; b) AST-GN95, REF 421982; c…

Biomerieux Inc

FDA Devices Critical May 1, 2024

Route 92 Medical Full Length 070 Access System, REF 7002, Rxonly, SterileEO. Used for Introduction of interventional devices into the neurovasculatur…

ROUTE 92 MEDICAL INC

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-52E

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

ACUSON Maple Diagnostic Ultrasound System, REF: 11711750, ACUSON Maple Select, REF: 11711779, running software version VA10A

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-58F

Howmedica Osteonics Corp.

FDA Devices Critical May 1, 2024

Route 92 Medical 070 Reperfusion System, REF 1003, Rxonly, SterileEO. Used for introduction of interventional devices into the neurovasculature and …

ROUTE 92 MEDICAL INC

FDA Devices Moderate May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20, 20 Tests

Quidel Corporation

FDA Devices Moderate May 1, 2024

Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.

Parker Laboratories, Inc.

FDA Devices Moderate May 1, 2024

Philips Patient Information Center (PIC) iX Uninterruptable Power Supply (UPS): 1. APC (Schneider Electric IT Corporation) 120V Uninterruptable Powe…

Philips North America Llc

FDA Devices Moderate May 1, 2024

TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 742-11-50D

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

3M Durapore Surgical Tape, Catalog Number 1538-118

3M Company - Health Care Business

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-44B

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-54E

Howmedica Osteonics Corp.

FDA Devices Moderate May 1, 2024

20" Lead Wires, Replacement Part Number: 1067724-2

EBI, LLC

FDA Devices Moderate May 1, 2024

Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga Chang Hydrodissection Cannulas. These Custom Paks are surgical procedure pac…

Alcon Research, LLC

FDA Devices Moderate May 1, 2024

Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the treatment of an established nonunion acquired secondary to trauma, exc…

EBI, LLC

FDA Devices Moderate May 1, 2024

Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog Number: EG-1000 Software Version: N/A Product Description: CLEANER bottles …

Electro Medical Systems SA

FDA Devices Moderate May 1, 2024

QUIDEL InflammaDry MMP-9 Test, REF: PRS-ID-20-U, 20 Tests

Quidel Corporation

FDA Devices Moderate May 1, 2024

ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System, REF: 11653093, running software v…

Siemens Medical Solutions USA, Inc.

FDA Devices Moderate May 1, 2024

Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x 23 cm (Symmetrical Tip, Heparin Coating and Tal VenaTrac Stylet- Intended for acut…

Covidien LP

NHTSA Critical May 1, 2024

HYUNDAI 2024: ENGINE AND ENGINE COOLING:EXHAUST SYSTEM:EMISSION CONTROL:GAS RECIRCULATION VALVE (EGR VALVE)

HYUNDAI

NHTSA Critical Apr 30, 2024

ALFA ROMEO 2021: FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS

ALFA ROMEO

NHTSA Critical Apr 29, 2024

NISSAN 2024: POWER TRAIN:DRIVELINE:DRIVESHAFT

NISSAN

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2024 across the FDA, CPSC 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 August 2026.