The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

451–475 of 32242

  • 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.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1200-2026·2026-08-12

    Smoked Pepper Cheese Varieties Recalled Due to Listeria monocytogenes Contamination

    Clover Hill Dairy, LLC is recalling Smoked Pepper Cheese Varieties (Jalapeno Cheddar) because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Smoked Pepper Cheese Varieties (Jalapeno 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 (Food)·H-1206-2026·2026-08-12

    Clover Hill Dairy LLP Mild Cheese Varieties Recalled Due to Listeria Contamination

    Clover Hill Dairy, LLC is recalling certain mild cheese varieties due to potential Listeria monocytogenes contamination.

    Product
    Clover Hill Dairy LLP, mild cheese variety (Snack Pack Assorted Regular Mild Stix White Colby, Marble Jack, Yummy Cheddar). 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 (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-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 (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-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-1220-2026·2026-08-12

    Requeson Cheese Recalled for Possible Listeria Contamination

    La Colonia Foods LLC is recalling 19 units of Requeson cheese packed in 18-lb buckets due to possible contamination with Listeria monocytogenes. The product was distributed to MD and VA.

    Product
    Requeson, bulk product from Clover Hill Dairy packed into a plastic 18-lb bucket. Unknown labeling information. Keep refrigerated.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-1204-2026·2026-08-12

    Clover Hill Dairy Soft Cuajada Crumbs Recalled for Listeria

    Clover Hill Dairy, LLC is recalling Soft Cuajada crumbs contaminated with Listeria monocytogenes. The product was distributed in MD, VA, and NY.

    Product
    Clover Hill Dairy LLP, Soft Cuajada crumbs. Unknown information: packaging, labeling, or total quantity of product distributed. Keep refrigerated.
    Category
    Food
    Distribution
    3 states
  • 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 (Devices)·Z-2879-2026·2026-08-12

    Boston Scientific Spinal Cord Stimulator Lead Kits Recalled

    Boston Scientific is recalling INFINION CX LEAD KITs (50cm and 70cm) used in spinal cord stimulator systems due to potential lead body stress at the anchor site, which may cause lead fractures or high impedance and result in inadequate stimulation or need for additional surgery.

    Product
    INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70, Material: M365SC2317700. part of the Boston Scientific Spinal Cord Stimulator (SCS) Systems.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·H-1210-2026·2026-08-12

    Clover Hill Dairy Sharp Cheese Snack Pack Sharp Stix Recalled Due to Listeria

    Clover Hill Dairy, LLC is recalling Sharp Cheese Snack Pack Sharp Stix (White or Yellow) because they may be contaminated with Listeria monocytogenes.

    Product
    Clover Hill Dairy LLP, Sharp Cheese Snack Pack Sharp Stix White or Yellow. 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 (Food)·H-1222-2026·2026-08-12

    Moringa Leaf Powder Dietary Supplement Recalled Due to Potential Salmonella Contamination

    Zen Principle Naturals Moringa Leaf Powder is being recalled because it may contain Salmonella. This affects specific lots of 900mg capsules.

    Product
    Zen Principle Naturals Moringa Leaf Powder dietary supplement, 900mg capsules, 180 capsules per PET white bottle. Intended Use: take 2 capsules per day. Route of Administration: OraI. Manufactured for Zen Principle 774 Mays Blvd Incline Village, NV 89451. The product is offered…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-1217-2026·2026-08-12

    La Colonia Foods Requeson Soft Ricotta Recalled Over Listeria Risk

    La Colonia Foods Llc is recalling 670 units of Salvadoreno Requeson Soft Ricotta due to possible Listeria monocytogenes contamination. The product was distributed in MD and VA.

    Product
    La Colonia Foods Salvadoreno Requeson Soft Ricotta, Net Wt: 14 oz (367g), packaged into retail-sized clear plastic containers. Keep refrigerated.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2798-2026·2026-08-12

    Halyard convenience kits containing Medline Namic manifolds recalled due to particulates

    AVID Medical, Inc. is recalling 5,168 Halyard convenience kits because they contain Medline Namic Angiographic Star Off Handle Manifolds that may have particulates in the fluid path.

    Product
    Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. HEART CATH, SELF REGIONAL SELF131-05
    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…
    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 (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-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-2897-2026·2026-08-12

    United Orthopedic U2 Knee Implant Bushings Recalled Over Engraving Design Issue

    United Orthopedic Corp. is recalling three Femoral offset bushing components of the U2 Total Knee System due to a design issue causing incorrect engraved numbering that could lead to incorrect implant orientation during surgery.

    Product
    Brand Name: U2 Total Knee System Product Name: Femoral offset bushing, 0mm and 4mm Model/Catalog Number: 9323-5310 Software Version: N/A Product Description: Manual Orthopedic Surgical Instrument Component: No, N/A
    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
  • SevereFDA (Devices)·Z-2909-2026·2026-08-12

    Blom-Singer Voice Prosthesis Boxes Mislabeled with Wrong Flange Type

    Freudenberg Medical is recalling 12 Blom-Singer Classic Indwelling Voice Prosthesis devices because the boxes are mislabeled, swapping Large Esophageal Flange and Large Esophageal and Tracheal Flange contents.

    Product
    Blom-Singer Classic Indwelling Voice Prosthesis, 16Fr/10 mm REF: 1610-LEF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide