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 9 critical, 40 moderate, and 1 lower-severity recalls. The page references 31 distinct recalling firms operating in 2 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (44), NHTSA (6), 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 Moderate Sep 25, 2024

Medline Contro-Bulb Syringe, REF DYND20125; bulb irrigation syringe

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Sep 25, 2024

vanSonnenberg Sump Locking Pigtail Regular Kit Sump Catheter System Kit, Material Number REF M001273090; for use as a percutaneously placed drain for intra-abdominal fluid collections.

Boston Scientific Corporation

FDA Devices Moderate Sep 25, 2024

STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095DA

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095D

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion device intended to stabilize a spinal segment to promote fusion using bone graft, in order to restrict motion and decrease pain. Users of these products are limited to physicians trained in orthopedic surgery. Clinical locations include hospitals and surgery sites equipped to perform spinal surgery. ii. TxTiHA The Innovasis TxTiHA IBF System is an intervertebral body fu

Innovasis, Inc

FDA Devices Moderate Sep 25, 2024

STREAMLINE BLOODLINE SET FOR DIALOG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7 M20 722233 Azurion 7 M12 722228 Azurion 5 M20 722227 Azurion 5 M12 722226 Azurion 7 B20 722225 Azurion 7 B12 722224 Azurion 7 M20 722223 Azurion 7 M12 722222 Azurion 3 M15 722221 Azurion 3 M12 722079 Azurion 7 M20 722078 Azurion 7 M12 722068 Azurion 7 B20 722067 Azurion 7 B12 722064 Azurion 3 M15 722063 Azurion 3 M12

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

STREAMLINE LONG-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095W

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus, REF DWM003A; anatomic total arthroplasty of the shoulder

Tornier, Inc

FDA Devices Moderate Sep 25, 2024

VariSoft Infusion Set, Single Use.

Unomedical A/S

FDA Devices Moderate Sep 25, 2024

Kits of Convenience containing 1 of the 2 Item Numbers: 1. Item Number: 59-300 HAWK Warming Grid, 2. Item Number: 59-320 HAWK Advanced Hypothermia Management Set. Convenience kits labeled as follows: Combat Life Saver - Intermediate (Product Number: 83-323-CB) contains 59-300 / 1 Each; Medic Enhancement Resupply (Product Number: 82-504-05) contains 59-300 / 1 Each; Combat Life Saver - Advanced (Product Number: 83-325-CB) contains 59-300 / 1 Each; Cold Weather (Product Number: 82-505)

Safeguard US Operating LLC

FDA Devices Moderate Sep 25, 2024

Alaris PCA Module Model 8120, a modular infusion pump and monitoring system

CareFusion 303, Inc.

FDA Devices Moderate Sep 25, 2024

Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system

CareFusion 303, Inc.

FDA Devices Moderate Sep 25, 2024

ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA; system, imaging processing, radiological

GE Healthcare GmbH

FDA Devices Moderate Sep 25, 2024

2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE CRM; b) 209031, Product Description: PROGRAMMER 209031 PORTABLE CRM; c) 2090AA, Product Description: PROGRAMMER 2090AA PORTABLE CRM; d) 2090AA4, Product Description: 2090AA4 PROGRAMMER-PORTABLE CRM; e) 2090AC, Product Description: SFTWR 2090AC PROGRAMMER-PORTABLE CRM W/; f) 2090AM, Product Description: PROGRAMMER CARELINK HONG KONG ASIA; g) 2090CHEN, Pro

Medtronic Inc.

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, High Volume Inlet, REF H938174, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

Atellica CH Microalbumin_2 (¿ALB_2)-For in vitro diagnostic use in the quantitative measurement of microalbumin in human urine on ADVIA Chemistry systems/ Atellica CH and Atellica CI Analyzers

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 25, 2024

Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and video EEG (vEEG) recordings and analysis. The Seer Home System includes the Sight Monitoring Hub, the Sense wearable, Monitoring Portal and associated accessory components (Disposable EEG Wires, WaterTabs, WaterTabs Application Kit, and Take-home Kit).

SEER MEDICAL PTY LTD

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV Cesar-Powerpack-Visub-Nicol 722021 INTEGRIS Allura 9 (biplane) 722018 Integris Allura 9 722017 Integris H5000 F / Allura 9F 722016 Integris H5000 C / Allura 9C

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument

Beckman Coulter, Inc.

FDA Devices Moderate Sep 25, 2024

regard Clinical Packaging Solutions, HT00376I - SPECIAL PROCEDURE, Item Number 800223009

ROi CPS LLC

FDA Devices Moderate Sep 25, 2024

BinaxNOW Respiratory Strep A Test Kit, CLIA Waived, Catalog Number 730025

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

ADVIA Chemistry Microalbumin_2 (¿ALB_2) -For in vitro diagnostic use in the quantitative measurement of microalbumin in human urine on ADVIA Chemistry systems/ Atellica CH and Atellica CI Analyzers.

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Sep 25, 2024

Flexima Regular Kit Biliary Catheter System Kit, Material Numbers REF M001271650; bile drainage catheter with locking pigtail

Boston Scientific Corporation

FDA Devices Moderate Sep 25, 2024

Acceava Respiratory Strep A, CLIA Waived, Catalog Number 4580295008

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Xper FD20/15 722039 Allura Xper FD20/20 OR Table 722038 Allura Xper FD20/20 722035 Allura Xper FD20 OR Table 722029 Allura Xper FD20/10 722028 Allura Xper FD20 722027 Allura Xper FD10/10 722026 Allura Xper FD10 722025 Allura Xper FD20 Biplane OR Table 722023 Allura Xper FD20 OR Table 722020 Allura Xper FD20 Biplane OR Table 722015 Allura Xper FD20 OR Table 722013 Allura Xper FD20 Biplane 722012 Allura Xper FD20 722011 Allura Xper FD1

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037 MultiDiagnost Eleva with Flat Detector 708036 MultiDiagnost Eleva 708034 MultiDiagnost Eleva with Flat Detector 708032 MultiDiagnost Eleva

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Sep 25, 2024

DIAMOND POINT, BOTH ENDS K-WIRE, REF 128042, metallic bone fixation fastener

Smith & Nephew, Inc.

FDA Devices Moderate Sep 25, 2024

Marodyne-LiV, part number 3045-133, Low intensity vibration exerciser supporting osteoporosis treatment

Btt Health Gmbh

FDA Devices Low Sep 25, 2024

BiomarC EX Fiducial Marker System, Catalog Number 040165

Carbon Medical Technologies, Inc.

FDA Devices Moderate Sep 25, 2024

Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument

Mazor Robotics Ltd

FDA Devices Moderate Sep 25, 2024

STREAMLINE BLOODLINE LONG VERSION, FMC-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095L

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system

CareFusion 303, Inc.

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Non-Vented, High Volume Inlet, REF H938173, for use in a pharmaceutical compounding device

Baxter Healthcare Corporation

FDA Devices Moderate Sep 25, 2024

ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood flow by effectively removing clots from occlusive vasculature in patients suffering from acute ischemic stroke.

MICROVENTION INC.

FDA Devices Moderate Sep 25, 2024

1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", sterile; 4. UNIMAX Detachable endo pocket, REF FEP936116, 3" x 6", sterile; 5. UNIMAX Detachable endo pocket, REF FEP979000, 8" x 10", sterile; 6. ConMed Corporation Detachable endo pocket, REF SB936, 3" x 6", steri

UNIMAX MEDICAL SYSTEMS INC

FDA Devices Moderate Sep 25, 2024

DIAMOND POINT, BOTH ENDS K-WIRE, REF 128062, metallic bone fixation fastener

Smith & Nephew, Inc.

FDA Devices Moderate Sep 25, 2024

AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036

B. Braun Medical, Inc.

FDA Devices Moderate Sep 25, 2024

General Purpose Syringe McKesson 60 mL Luer Lock Tip Without Safety, Catalog Number 869662, McKesson Brand Catalog Number: 102-S60C

Cypress Medical Products LLC

FDA Devices Moderate Sep 25, 2024

STREAMLINE BLOODLINE SET FOR DIALOG DR-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2010M2096A

B Braun Medical Inc

FDA Devices Moderate Sep 25, 2024

Flexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF M001271960, b) REF M001271970; all-purpose drainage catheter with locking pigtail

Boston Scientific Corporation

FDA Devices Moderate Sep 25, 2024

GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c) 2110344-010; d) 2110344-011; e) 2110344-013; f) 2110344-019; g) 2110344-025; h) 2110344-029; i) 2110344-030; j) 2110344-032 ; Radiological image processing system

GE Healthcare

FDA Devices Moderate Sep 25, 2024

ViewPoint; system, imaging processing, radiological

GE Healthcare GmbH

NHTSA No agency class Sep 25, 2024

BMW,MINI 2023-2025: STRUCTURE:BODY

BMW,MINI

NHTSA No agency class Sep 25, 2024

BUICK 2024: EQUIPMENT:OTHER:LABELS

BUICK

NHTSA No agency class Sep 24, 2024

ASTON MARTIN 2025: ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:PIPES, HOSES, AND FITTINGS

ASTON MARTIN

NHTSA No agency class Sep 20, 2024

TOYOTA 2023-2025: SERVICE BRAKES, ELECTRIC:SOFTWARE/PROGRAMMING

TOYOTA

NHTSA No agency class Sep 20, 2024

MERCEDES-BENZ 2021-2023: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM):SOFTWARE

MERCEDES-BENZ

NHTSA No agency class Sep 20, 2024

NISSAN 2019-2020: ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY

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: 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.