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 8 critical, 41 moderate, and 1 lower-severity recalls. The page references 29 distinct recalling firms operating in 5 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (36), FDA Food (9), NHTSA (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, 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 Jul 10, 2024

Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 50-80mm Model/Catalog Number: MR2102050 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate Jul 10, 2024

BD Pyxis, Name/REF: BD PYXIS MB TOWER MAIN/ 169-153, BD PYXIS MB TOWER MAIN CR/ 169-154, BD PYXIS MB TOWER MAIN W/MP/ 169-157, BD PYXIS MB TWR MN 1FM-10HH-1FH MP/ 169-143, BD PYXIS MB TWR MN 2FH-1FM-4HH-2FM MP/ 169-145, BD PYXIS MB TWR MN 2FM-8HH-1FH MP/ 169-144, BD PYXIS MB TWR MN 4FH-4HH-1FM MP/ 169-142, BD PYXIS MB TWR RXNOW MAIN W/MED PRINTER / 169-155, BD PYXIS MB TWR RXNOW MAIN W/PAT PRINTER/ 169-156, BD PYXIS MDBANK TWR MN 7HH-1HM-3FM/ 169-132, BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow/ 1

CareFusion 303, Inc.

FDA Devices Moderate Jul 10, 2024

First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.

First Source Inc

FDA Devices Moderate Jul 10, 2024

DxI 9000 Access Immunoassay Analyzer, C11137; in-vitro diagnostic

Beckman Coulter, Inc.

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kit: Medline Neuro IR Pack, Pack #DYNJ56073C, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

The Non-Sterile Flyte hood covers the user s head and neck region and is intended to be worn with commercially available gowns. The hood is donned after the Flyte helmet and before the gown, such that the hood is securely tucked inside the gown. The hood attaches to and covers the helmet and air is drawn into the helmet through a filter located on the top-backside of the hood. The filtered air is delivered into the helmet and the disposable does not inhibit adjustment of helmet settings/function

Stryker Corporation

FDA Devices Moderate Jul 10, 2024

Neurostimulation Kit (Ported, Dual 8, 40 cm), REF: 71005-US Peripheral Nerve Stimulation Kit (Ported, Dual 8, 40 cm), REF: 71019-US Components of the Nalu Spinal Cord Stimulation System.

Nalu Medical, Inc.

FDA Devices Low Jul 10, 2024

VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate the VITROS 5,1 FS/4600 Chemistry Systems and the VITROS 5600/XT 7600 Integrated Systems for the quantitative measurement of total iron-binding capacity (TIBC) using VITROS Chemistry Products dTIBC Reagent Model/Catalog Number: 6802344

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Jul 10, 2024

BD Alaris System Manager REF: 9601, compatible with BD Alaris PC Units

CareFusion 303, Inc.

FDA Devices Moderate Jul 10, 2024

Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY

Abbott Medical

FDA Devices Moderate Jul 10, 2024

IsoLoc Prostate Immobilization Treatment Balloon Device Kit, Catalog/UPN: ISO-100

Angiodynamics, Inc.

FDA Devices Moderate Jul 10, 2024

Brand Name: Fathom Pedicle-Based Retractor Product Name: C/C Blade, 35-55mm Model/Catalog Number: MR2102035 Product Description: Cranial Caudal Blade Component: Yes, a component of a retractor blade

SEASPINE ORTHOPEDICS CORPORATION

FDA Devices Moderate Jul 10, 2024

Stryker Sustainability Solutions, BW Lasso 2515 NAV eco Variable Diagnostic EP Catheter, REF: D134301, ELECTRODES: 22, spacing:2-6-2MM, Length 115 cm, STERILE.EO, Rx Only

Stryker Sustainability Solutions

FDA Devices Moderate Jul 10, 2024

Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation, Pack #ACC010254B, containing a Pure Pouch component DYND04000, O.R. Scissors S/B, 5.5 Sterile. b. Medline Code Cart Drawer 2 Adult Kit, Pack ACC010365A, containing a Pure Pouch component DYNJ04048, Kelly Forceps/STD STR Sterile. c. Medline Code Cart Drawer 2 Adlt Peds, Pack #ACC010366A, containing a Pure Pouch component DYNJ04048, Kelly Forceps/STD STR Sterile. d. Medline Drawer 2, Pack #ACC010375A, containing a

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

Non-sterile convenience kits: Medline Open Heart CDS, Pack #CDS981759C, containing a Pure Pouch with component Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kits: a. Medline Cath Lab Special Procedure, Pack #00-RDF0360, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile. b. Medline Angiography Pack, Pack #DYNJ26488W, containing a Pure Pouch with component Medline Reorder #DYNJ04048, Kelly Forceps/STD STR Sterile. c. Medline Heart Catheterization Pack, Pack #DYNJ30927Q, containing a Pure Pouch with component Medline O.R. Scissors, S/B, 5.5 Sterile Scissors, Reorde

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

EasySuite 4K Integrated Operating Room System Model/Catalog Number: EasySuite 4K- The EasySuite 4K system includes a touch panel user interface for quick routing of 2K/4K procedural video to displays within the operating room and for convenient control of room video cameras, surgical cameras, ambient lighting, and surgical lights.

Olympus Corporation of the Americas

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA 2000" Patient Return Electrode Product Name: MEGADYNE" MEGA 2000" Patient Return Electrode Model/Catalog Number: 0800 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega 2000, Adult, For Patients Weighing over 25lbs. (11.4Kg), 91cm Long x 51cm Wide Component: No

Megadyne Medical Products, Inc.

FDA Devices Moderate Jul 10, 2024

Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

Exactech, Inc.

FDA Devices Moderate Jul 10, 2024

Nonsterile convenience kits: a. Medline Delivery, Pack #DYNJ901130I, containing a Pure Pouch with component Reorder #DYND04000, O.R. Scissors, S/B, 5.5 Sterile. b. Medline C-Section, Pack DYNJ902938J, containing a Pure Pouch with component Reorder #DYND04000, O.R. Scissors, S/B, 5.5 Sterile.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

Sterile convenience kit: Medline Birthing Room Pack, Pack #DYNJ38429D, containing a Pure Pouch component Sterile Sharp/Blunt Scissors 5.5", Reorder #65945 and containing a Pure Pouch component Sterile 5.5" Episiotomy Scissors, Reorder #67645.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Moderate Jul 10, 2024

Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion Pumps

Zyno Medical LLC

FDA Devices Moderate Jul 10, 2024

This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then inserted into the cannula. Catalog Number: 0406-630-225

Stryker Corporation

FDA Devices Moderate Jul 10, 2024

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

Applied Medical Technology Inc

FDA Devices Moderate Jul 10, 2024

Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the ability to inject bone cement into multiple different areas through a single point of access in the patient. Catalog Number: 1025-011-500

Stryker Corporation

FDA Devices Moderate Jul 10, 2024

VITROS Chemistry Products FS Diluent Pack 3, Model/Catalog Number: 6801754. Product Description: VITROS Chemistry Products FS Diluent Pack 3 comes with 3 packs per sales unit.

Ortho-Clinical Diagnostics, Inc.

FDA Devices Moderate Jul 10, 2024

WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith & Nephew Inc. REF Numbers: T0449-01

WOM World Of Medicine AG

FDA Devices Moderate Jul 10, 2024

Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete photometric chemistry analyzer for clinical use. It is an in-vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids with Catalog Number C11137.

Beckman Coulter, Inc.

FDA Devices Moderate Jul 10, 2024

HORIBA custom configured fluorescence instrument, modular Fluorolog-QM

Horiba Instruments Incorporated

FDA Devices Moderate Jul 10, 2024

ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.

Siemens AG/Siemens Healthcare GmbH

FDA Devices Moderate Jul 10, 2024

Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF, Pack #DYNJ47873L, containing a Pure Pouch with component Sterile Curved Kelly Hemostat, Reorder #66175.

MEDLINE INDUSTRIES, LP - Northfield

FDA Devices Critical Jul 10, 2024

Brand Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Product Name: MEGADYNE" MEGA SOFT" Dual Reusable Patient Return Electrode Model/Catalog Number: 0835 Software Version: N/A Product Description: Reusable Patient Return Electrode, Mega Soft, Dual Cord, Adult, For Patients Weighing over 25lbs. (11.4kg), 117cm Long x 51cm Wide x 1.25cm Thick Component: No

Megadyne Medical Products, Inc.

FDA Devices Moderate Jul 10, 2024

First Source iQ Flex M. Portable cart and platform that supports an X-ray system and laptop computer.

First Source Inc

FDA Devices Moderate Jul 10, 2024

Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and ComboLab AltiX hemodynamic and electrophysiology recording system; and Field Replacement Units spare part #5875569 (Assy CLABIII AMP 128CH 100-240V 50-60HZ).

GE Medical Systems Information Technologies Inc

FDA Devices Moderate Jul 10, 2024

Avalon Ultrasound Transducer. Directs low-energy ultrasound beam toward the fetal heart and externally monitors fetal heart rate.

Philips North America Llc

FDA Devices Moderate Jul 10, 2024

EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.

MicroPort Orthopedics Inc.

USDA FSIS Moderate Jul 10, 2024

FSIS Issues Public Health Alert for Ineligible Meat and Poultry Products Illegally Imported from the Philippines

NHTSA No agency class Jul 9, 2024

MERCEDES-BENZ 2023-2024: SUSPENSION:REAR:SPRINGS:LEAF SPRING ASSEMBLY:U-BOLT, LEAF SPRING TO AXLE

MERCEDES-BENZ

NHTSA No agency class Jul 8, 2024

MERCEDES-BENZ 2023: STRUCTURE:INTERIOR PANELS:DASHBOARD

MERCEDES-BENZ

NHTSA No agency class Jul 8, 2024

JEEP 2021-2022: AIR BAGS:SIDE/WINDOW:CURTAIN

JEEP

USDA FSIS Critical Jul 5, 2024

Al-Safa US LLC Recalls Frozen Ready-To-Eat Chicken Products Due to Possible Listeria Contamination

FDA Food Moderate Jul 3, 2024

Cream Cheese Stuffed Plain Mini Bagels

FEEL GOOD FOODS INC

FDA Food Moderate Jul 3, 2024

(Item 551697) Wakefield Ham & Cheddar Pretzel Croissant

Classic Delight LLC

FDA Food Critical Jul 3, 2024

Green Life Farms Baby Arugula in 4.5 ounce plastic clamshell packaging containers. 6 packages per case of 4.5oz each. Store in refrigerator.

GREEN LIFE FARMS

FDA Food Moderate Jul 3, 2024

(Item 73131) Turkey Sausage & Egg Muffin

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 514711) Wakefield Bacon, Egg & Cheese Bagel

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 195263) Wakefield Spicy Hawaiian Sliders

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 806679) Wakefield Charbroiled Cheeseburger

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

Universal Bakery Organic Aussie Bites, 30 oz clamshell container

Best Express Foods, Inc.

FDA Food Critical Jul 3, 2024

Pop a Nosh Mixed Munch; Regular Flavor; 8oz plastic bag; Potato Chips, Popcorn, Pretzels; UPC 914669941

AMB FOODS 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.