The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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176–200 of 36486

  • SevereFDA (Drugs)·D-0745-2026·2026-08-12

    FDA Recalls Mirabegron Tablets Over Nitrosamine Impurity

    Zydus Pharmaceuticals is recalling Mirabegron extended-release tablets, 25 mg, due to an out-of-specification result for the N-Nitroso Mirabegron impurity. The recall affects nationwide distribution in the USA.

    Product
    MIRABEGRON — MIRABEGRON (MIRABEGRON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2857-2026·2026-08-12

    OXOS Medical Recalls MC2 Portable X-Ray Systems Over Circuit Board Overheating

    OXOS Medical Inc is recalling 77 units of the MC2 Portable X-Ray System due to a defective circuit board that overheats. The recall affects devices distributed nationwide in FL, GA, IN, SC, TX, and VA.

    Product
    Brand Name: OXOS Medical, Inc Product Name: MC2 Portable X-Ray System Model/Catalog Number: MC2, MC2.1 Software Version: 5.7.0 Product Description: The MC2 Portable X-Ray System ( MC2 System or MC2 ) is a portable and handheld x-ray system designed to aid clinicians with po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1213-2026·2026-08-12

    Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling various Pepper Jack cheese varieties because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Jalapeno Cheddar, Pepper Jack, Sizzlin Colby with Habanero Peppers). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refr
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2876-2026·2026-08-12

    GE Healthcare MAC VU360 Electrocardiograph Software Recall

    GE Healthcare is recalling 163 MAC VU360 electrocardiograph units due to a software issue that may cause a previous patient's data to remain visible and be incorrectly associated with a subsequent patient.

    Product
    GE Healthcare MAC VU360, REF# part number 2030361-023; Electrocardiograph
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1218-2026·2026-08-12

    Salvadorean Cheese Recalled for Possible Listeria Contamination

    La Colonia Foods LLC is recalling Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese (14 oz) due to possible contamination with Listeria monocytogenes.

    Product
    Selectos Latinos Requeson Salvadoreno Ricotta Style Salvadorean Cheese, Net Weight 14 oz, packed into retail-sized clear plastic containers. Keep refrigerated.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0744-2026·2026-08-12

    Cyclophosphamide Injection Recall: Stainless Steel Particulate Matter Found

    Cyclophosphamide for Injection, USP, 2 gram/vial, is being recalled due to the presence of particulate matter identified as stainless steel. The recall affects 1,464 vials distributed nationwide.

    Product
    Cyclophosphamide for Injection, USP, 2 gram/vial, One Single-Dose Vial, Rx only, Manufactured for: Long Grove Pharmaceuticals, LLC, Rosemont, IL 60018. Manufactured in Taiwan, NDC 81298-8114-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2843-2026·2026-08-12

    Powered Wheelchair Controller Software Recall by Pride Mobility

    Pride Mobility is recalling 1,102 Q6 Edge 3 Stretto powered wheelchairs with controller software version 2.0.11 due to a defect that may cause unexpected brake stops or control system crashes.

    Product
    Brand Name: Quantum Rehab Product Name: Q6 Edge 3 Stretto Model/Catalog Number: Q6 Edge 3 Stretto Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1208-2026·2026-08-12

    Fresh Cheddar Curd Cheese Recalled Due to Listeria Contamination

    Clover Hill Dairy's Fresh Cheddar Curd cheese is recalled due to Listeria monocytogenes contamination. The product was distributed in Maryland, Virginia, and New York.

    Product
    Clover Hill Dairy LLP, mild cheese variety (Fresh Cheddar Curd). Sold in approximate 0.75-lb and 1.5-lb box units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-1212-2026·2026-08-12

    Clover Hill Dairy Flavored Cheese Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling Old Bay Cheddar flavored cheese because it may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Flavored Cheese (Old Bay Cheddar). Sold in approximate 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-1215-2026·2026-08-12

    Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling Pepper Jack Cheese Varieties due to potential Listeria monocytogenes contamination.

    Product
    Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (3-in-a-Pack Assorted Jalapeno Cheddar, Pepper Jack, Sizzling Colby). Sold in approximate 0.20-lb (3.2oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2891-2026·2026-08-12

    Philips Allura X-Ray Systems Recalled Over Unauthorized Hard Disk Drives

    Philips is recalling 5,012 Allura interventional fluoroscopic X-ray systems nationwide due to potential loss of imaging functionality, motorized movement, or data caused by unauthorized hard disk drives.

    Product
    Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1216-2026·2026-08-12

    Smoked Cheddar Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy is recalling its smoked cheddar cheese varieties because they may be contaminated with Listeria monocytogenes. The products were sold in Maryland, Virginia, and New York.

    Product
    Clover Hill Dairy LLP, Smoked Cheddar Cheese Varieties (Cheddar, White Cheddar). Sold in 1/2-lb and 1-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2840-2026·2026-08-12

    Radial Jaw 4 Jumbo Biopsy Forceps Packaging Sterile Barrier Recall

    Boston Scientific is recalling Radial Jaw 4 Jumbo Biopsy Forceps due to potential breach in the sterile barrier of device packaging. The recall affects 5,020 units in the US and 20,770 units outside the US.

    Product
    Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1199-2026·2026-08-12

    Clover Hill Dairy Soft Ricotta Recalled Due to Listeria Contamination

    Clover Hill Dairy is recalling Soft Ricotta and Soft Ricotta with Jalapenos due to Listeria monocytogenes contamination. Products were distributed in MD, VA, and NY.

    Product
    Clover Hill Dairy LLP, Soft Ricotta (Requeson), and Soft Ricotta with Jalapenos (Requeson Con Chile). Sold in 2- and 5-gallon buckets, and 10oz, 12oz, and 14oz individually packaged food grade clamshell containers. The 5- and 2-gallon buckets are shrink wrapped. Keep refrigerated
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2854-2026·2026-08-12

    Copan WASPLab Software Recall Over Results Overwrite Issue

    Copan WASP is recalling WASPLab devices due to a software issue in the WebApp that may prevent users from overwriting results. The recall affects WebApp versions 2.33.1, 2.33.3, and 2.34.2.

    Product
    Brand Name: WASPLab Product Name: WASPLab Model/Catalog Number: W087 Software Version: WebApp version 2.33.1, 2.33.3 and 2.34.2 Product Description: WASPLab is an automated device intended to be used for the incubation and the digital imaging of agar culture plates streaked w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2889-2026·2026-08-12

    Beckman Coulter MicroScan Panel Update DVD Kits Recalled

    Beckman Coulter is recalling MicroScan LabPro V5.03 Panel Update 11 DVD Kits due to incorrect algorithms that may affect antimicrobial susceptibility test results, potentially leading to false susceptibility classifications.

    Product
    REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following instruments: - B1018-280 MicroScan autoSCAN-4 Instrument - B1018-283 MicroScan WalkAway-40 plus Instrument - B1018-284 MicroScan WalkAway-96 plus Instrument - B1018-440 DxM-1040 MicroScan Walk
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2900-2026·2026-08-12

    GEM Premier 5000 PAK Lysing Solution Concentration Recall

    Specific lots of the GEM Premier 5000 PAK lysing bag solution have an active ingredient concentration that does not meet manufacturing specifications, which could delay recognition and management of Co-Oximetry and total bilirubin abnormalities.

    Product
    GEM Premier 5000 PAK Part Numbers: 00055360010 00055360011 00055407504 00055415010 00055430010 00055430011 00055445010 00055445011 00055360010.A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2862-2026·2026-08-12

    Stryker AHTO Tube Set Packaging Recalled for Handpiece Leaking

    Stryker is recalling 46,212 units of its AHTO Tube Set Packaging (Catalog Number 0250070600) due to reported complaints of leaking from the handpiece during use. The recall affects products distributed worldwide, including US Nationwide and multiple countries.

    Product
    STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2835-2026·2026-08-12

    Therabody Theragun G4 PRO Charger Recalled for Fire Risk

    Therabody is recalling Theragun G4 PRO chargers because they may overheat, presenting a risk of fire, smoke, or melting.

    Product
    Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1201-2026·2026-08-12

    Soft Cuajada in Brine Recalled Due to Listeria monocytogenes Contamination

    Clover Hill Dairy, LLC is recalling Soft Cuajada in Brine because it may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Soft Cuajada in Brine, sold in five (5) gallon and two (2) gallon buckets. Unknown information: labeling. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-1214-2026·2026-08-12

    Clover Hill Dairy Pepper Jack Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling certain Pepper Jack Cheese Varieties because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Pepper Jack Cheese Varieties (Snack Pack Assorted Pepperjack Stix (Jalapeno Cheddar, Pepper Jack)). Sold in approximate 0.40-lb (6.4oz) units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2875-2026·2026-08-12

    Merge OrthoPACS Imaging Workstation Recall for Patient Data Display Issue

    Merge Healthcare is recalling 5 units of its Merge OrthoPACS medical imaging diagnostic workstation due to a software issue where thumbnails from a previously opened patient study may appear while a different patient study is currently open.

    Product
    Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2856-2026·2026-08-12

    Powered Wheelchair Control Software Recall by munevo

    Munevo is recalling 19 powered wheelchair hands-free control systems due to a software issue that may cause the driving mechanism to fall out of calibration, leading to unexpected steering drift or imprecise control.

    Product
    munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1205-2026·2026-08-12

    Clover Hill Dairy Mild Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling various mild cheese varieties because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Mild Cheese Variety (Yummy Cheddar, White Cheddar, White Colby, Monterey Jack, Marble Jack). Sold in 1/2-lb, 1-lb, 2.5-lb, 5-lb, and 40-lb units. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·26V526000·2026-08-12

    Nissan Recalls 2025 Altima Vehicles Due to Air Bag Fastener Defect

    Nissan is recalling 2025 Altima vehicles because incorrect mounting fasteners may prevent front passenger air bags from deploying as intended in a crash.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide