PlainRecalls

2024 Recalls

6,210 recalls · Page 63 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 3 critical, 46 moderate, and 1 lower-severity recalls. The page references 28 distinct recalling firms operating in 3 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (35), FDA Food (8), FDA Drug (7), 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 Food Moderate Jul 3, 2024

(Item 176594) Wakefield Southern Chicken Biscuit

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

Fresh Catch Inc. Yellowfin Tuna, 1 loin per case packaged in carboard boxes with keep refrigerated label

Fresh Catch Inc

FDA Food Critical Jul 3, 2024

Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and Niwali Mexican

GLOBAL MIX INC.

FDA Food Moderate Jul 3, 2024

(Item 7060) Classic Delight Chili Cheese Dogs

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 6731) Classic Delight Turkey & Cheese On Round Bun - INSTITUTIONAL USE ONLY

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 648899) Wakefield Chorizo & Egg on Ciabatta

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

(Item 806687) Wakefield Chicken & Cheese Kaiser Roll

Classic Delight LLC

FDA Food Moderate Jul 3, 2024

Chef Select 2 Herb Baguettes Filled With Herb Butter 2x175 g Barcode: 4056489447566. Frozen product packaged in a plastic bag, 2 baguettes per unit.

Lidl US TRADING

FDA Drug Moderate Jul 3, 2024

Zilretta (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only, Manufactured for: Pacira Pharmaceuticals Inc., Sa…

PACIRA PHARMACEUTICALS INC

FDA Drug Moderate Jul 3, 2024

Labetalol Hydrochloride Injection, USP, 20 mg/4 mL (5 mg/mL), 4 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intravenous Inje…

Pfizer Inc.

FDA Drug Moderate Jul 3, 2024

Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with Luer Lock, For Intramuscular or Intrav…

Pfizer Inc.

FDA Drug Moderate Jul 3, 2024

Extra Strength Acetaminophen 500 MG Tablets,100-count Bottle, Distributed By: MAJOR PHARMACEUTICALS, 17177 N Laurel Park Drive, Suite 233, Livonia, M…

Contract Pharmacal Corporation

FDA Drug Moderate Jul 3, 2024

Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, a) 30 capsules bottles, NDC 60429-165-30; b) 90 capsules bottles, NDC 60429-165-90, Mfr. by:…

Golden State Medical Supply Inc.

FDA Drug Moderate Jul 3, 2024

Progesterone 200 mg, Compounded, 90-count bottle, Rx, Dissolve One Sublingual Tablet After Dinner Nightly, AnazaoHealth, 5710 Hoover Blvd, Tampa, Fl …

Coast Quality Pharmacy, LLC dba Anazao Health

FDA Drug Low Jul 3, 2024

SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12 Hour Relief, 0.5 fl oz (15 ml…

Neilmed Pharmaceuticals Inc

FDA Devices Moderate Jul 3, 2024

EVERA MRI S VR SureScan, Model Number DVMC3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

COBALT DR MRI SureScan, Model Number DDPB3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

COBALT HF QUAD CRT-D MRI SureScan, Model Number DTPB2QQ, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

NovaGuide 2 Traditional Ultrasound , REF: NSC-TCDNG2

NovaSignal Corp.

FDA Devices Moderate Jul 3, 2024

Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

COBALT XT VR MRI SureScan, Model Number DVPA2D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

The VASOVIEW HemoPro 2 Endoscopic Vessel Harvesting System, labeled as the following: 1. VasoView Hemopro 2, Model Number: VH-4000. 2. VasoView Hem…

Maquet Cardiovascular, LLC

FDA Devices Moderate Jul 3, 2024

2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401, L201-90411, L201-90421, part of the…

Thoratec Switzerland GMBH

FDA Devices Moderate Jul 3, 2024

MIRRO MRI VR SureScan, Model Number DVME3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

CARESCAPE Canvas 1000, Model Numbers: a) 5865770; b) 5865770-01040169; c) 5865770-01054142; d) 5865770-01054696; e) 5865770-01054698; f) 58657…

GE Healthcare Finland Oy

FDA Devices Moderate Jul 3, 2024

CARESCAPE Canvas Smart Display, Model Numbers: a) 5514418, b) 5514418 / MAEP2, c) 5514418-01059642, d) 5514418-01080402, e) 5514418-01081317,…

GE Healthcare Finland Oy

FDA Devices Moderate Jul 3, 2024

AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient de…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Siemens Material Number: 11416751 RAPIDPoint 500e Blood Gas System (China) 114…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate Jul 3, 2024

The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The disposable system consists of an ou…

Mermaid Medical A/S

FDA Devices Moderate Jul 3, 2024

Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.

Stryker GmbH

FDA Devices Moderate Jul 3, 2024

COBALT DR MRI SureScan, Model Number DDPB3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

CROME VR MRI SureScan, Model Number DVPC3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Sight OLO CBC Test Kit, Model/Catalog Number: TK1. A disposable cartridge and sample preparation tools for use with the Sight OLO CBC analyzer.

SIGHT DIAGNOSTICS LTD

FDA Devices Moderate Jul 3, 2024

CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and har…

Integra LifeSciences Corp.

FDA Devices Moderate Jul 3, 2024

CARESCAPE B850 Model Numbers: a) MBC303, Model Numbers: 1) 2078633-001, 2) 2078633-010, 3) 2078633-012, 4) 2078633-017, 5) 2078633-028, 6) …

GE Healthcare Finland Oy

FDA Devices Moderate Jul 3, 2024

MIRRO MRI DR SureScan, Model Number DDME3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Critical Jul 3, 2024

Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and B…

Baxter Healthcare Corporation

FDA Devices Moderate Jul 3, 2024

CARESCAPE B650: Model Numbers: a) MBB313, Model Numbers: 1) 2095801-001, 2) 2095801-001-01018416, 3) 2095801-001-01023150, 4) 2095801-001-010…

GE Healthcare Finland Oy

FDA Devices Critical Jul 3, 2024

SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567…

Philips North America Llc

FDA Devices Moderate Jul 3, 2024

MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP S…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 3, 2024

NovaGuide 2 Intelligent Ultrasound, REFs: NSC-NVGSYS2 & NSC-NVGSYS2-CA

NovaSignal Corp.

FDA Devices Moderate Jul 3, 2024

COBALT VR MRI SureScan, Model Number DVPB3D4, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Infinity Acute Care System (IACS) Monitoring System, Infinity M500 with Power, Model No. MS20407. Rev 20, 21, and 23

Draeger Medical Systems, Inc.

FDA Devices Moderate Jul 3, 2024

Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. …

Dental EZ Group Star Dental Division

FDA Devices Moderate Jul 3, 2024

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Centers For Disease Control and Prevention

FDA Devices Moderate Jul 3, 2024

PRIMO MRI DR SureScan, Model Number DDMD3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S -PG5F90S018 -PG6F45HS -PG6…

Merit Medical Systems, Inc.

FDA Devices Moderate Jul 3, 2024

MIRRO MRI VR SureScan, Model Number DVME3D1, Implantable Cardioverter Defibrillator

Medtronic Inc.

FDA Devices Moderate Jul 3, 2024

Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101

ASPEN SURGICAL

FDA Devices Moderate Jul 3, 2024

COBALT XT HF CRT-D MRI SureScan, Model Number: DTPA2D1, Implantable Cardioverter Defibrillator

Medtronic 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: 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.