The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

22051–22075 of 50429

  • HighFDA (Devices)·Z-3043-2020·2020-10-07

    Ameditech Recalls QuickTox Drug Screen DipCards Due to Performance Failures

    Ameditech is recalling QuickTox Drug Screen DipCards because immunoassay enzymes failed performance tests, meaning the products may not consistently detect all compounds at labeled levels.

    Product
    QuickTox Drug Screen DipCard(AMT Item/ AMT Description): QT70/ "QuickTox¿ Drug Screen Dipcard 11 Drug Detection: COC300+OPI300+MET500+THC50+AMP1000+PCP25+BZO300+BAR300+MTD300+OXY100+MDMA500", QT88/ "QuickTox¿ Drug Screen Dipcard 12 Drug Detection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0006-2021·2020-10-07

    Endo GIA Auto Suture Universal Articulating Loading Unit Recall

    FDA is recalling Endo GIA Auto Suture Universal Articulating Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.

    Product
    Endo GIA Auto Suture Universal Articulating Loading Unit 45 mm - 3.5 mm, Item Code 030455 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0002-2021·2020-10-07

    Shatto Milk Company Recalls Ice Cream Sandwiches for Undeclared Soy Allergen

    Shatto Milk Company is recalling Choc + Chip ice cream sandwiches because the cookie portion contains undeclared soy lecithin, a major food allergen.

    Product
    Shatto Milk Company, Choc + Chip, Chocolate Chip Cookie and Vanilla Ice Cream Sammich, Net Wt. 4.5 oz, Shatto Milk Company, Osborn, MO
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-3019-2020·2020-10-07

    Exactech Recalls Equinoxe Reverse Shoulder Compression Screw Kits

    Exactech is recalling Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kits because they may contain screws of incorrect length.

    Product
    Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-3030-2020·2020-10-07

    Ameditech Recalls Alere iScreen Multi Drug Detection Tests

    Ameditech is recalling Alere iScreen Multi Drug Detection tests because they may fail to consistently detect all compounds at labeled levels.

    Product
    Alere iScreen Multi Drug Detection (AMT Item Number/ AMT Description): X11-IS12-DX / "Alere iScreen" Dx Multi-Drugs of Abuse Dip Test 12 Drug Detection:AMP1000+BAR300+BZO300+COC300+THC50+MTD300+MET500+MOP300+OXY100+PCP25+MDMA500+TCA1000", X11-IS12-DX / "Alere iScreen" Dx…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0038-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,260 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" P-11 SVP2295, UDI: 20884521177410 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0020-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,264 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36" GS-12, Cutting Product Number: CV486, UDI: 20884521150925 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3032-2020·2020-10-07

    Ameditech Recalls CLIA Waived Rapid Drug Tests for Performance Failures

    Ameditech Inc is recalling various CLIA Waived Rapid Drug Tests because immunoassay enzymes failed performance standards, preventing consistent detection of compounds.

    Product
    CLIA Waived Rapid Drug Test (AMT Item Number/ AMT Description): X07-CLIA-SDDT-25 / CLIA Waived" Inc. Single Drug Dipstick Test BUP10, X07-CLIA-SDDT-25 / "CLIA Waived" Inc. Single Drug Dipstick Test BUP10, X07-CLIA-SDDT-13 /"CLIA Waived" Inc. Single Drug Dipstick Test…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0018-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 8,598 units of non-sterile Velosorb sutures because use could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" CV-25 Taper, Product Number: CV3110, UDI: 20884521150918 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1621-2020·2020-10-07

    Cretors Organic Olive Oil Popcorn Recalled for Potential Glass Contamination

    Eagle Family Foods Group is recalling Cretors Organic Extra Virgin Olive Oil Popcorn because pieces of glass may be present in the product.

    Product
    Cretors Organic Extra Virgin Olive Oil Popcorn, 4.4 oz. bag, UPC 732494001170, 12 retail units per wholesale case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0010-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 7,969 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 6/0 Undyed 18" P-10 Cutting, Product Number: SV9913, UDI: 20884521153278 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0002-2021·2020-10-07

    Endo GIA Stapler Loading Units Recalled for Staple Formation Defects

    FDA recalls Endo GIA Auto Suture Loading Units because staples may not form properly, potentially preventing adequate hemostasis during surgery.

    Product
    Endo GIA Auto Suture Universal Articulating Loading Unit 30 mm - 2.5 mm, Item Code 030451 - Product Usage: The Endo GIA universal staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0027-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 3,103 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. This defect could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36" GS-21 Taper, Product Number: CV947, UDI: 20884521153056 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0024-2021·2020-10-07

    Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling non-sterile Velosorb sutures that could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" CV-25 Taper, Product Number: CV3100, UDI: 20884521150901 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0041-2021·2020-10-07

    Riverpoint Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 1,236 units of non-sterile Velosorb sutures due to risks of surgical site infection and compromised sterile fields.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30" PC-11 SV487G, UDI: 10884521149595 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0046-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 7,496 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile, posing a risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30" P-12 Cutting SV426, UDI: 20884521151731 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0042-2021·2020-10-07

    Riverpoint Medical Recalls Non-Sterile Velosorb Surgical Sutures

    Riverpoint Medical is recalling 3,109 units of Velosorb Fast Braided Absorbable Sutures because they are non-sterile. The defect could compromise the sterile field and increase the risk of surgical site infection.

    Product
    Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36" GS-25 CV605, UDI: 20884521152295 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V615000·2020-10-06

    Motorhome propane stove gas leak recall affects 2020-2021 models

    REV is recalling certain 2020-2021 Fleetwood and Holiday Rambler motorhomes with Dometic propane stoves due to potential gas leaks that could increase fire risk. Owners should contact REV for free repair at 1-800-509-3417.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD ADMIRAL, FLAIR, BOUNDER, SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E075000·2020-10-06

    TriMark Recalls 50-200 Door Latches for Emergency Vehicles

    TriMark is recalling 50-200 door latches used in emergency vehicles because trip levers may fail, preventing doors from opening.

    Product
    LATCHES/LOCKS/LINKAGES:DOORS:LATCH recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E074000·2020-10-06

    Lippert Components Recalls Electric Motors in Power Bedlift Systems

    Lippert Components is recalling electric motors in Power Bedlift systems because internal gear failure may cause the bed to extend unexpectedly, increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V617000·2020-10-06

    Vespa GTS 300 and GTV 300 Scooters Recalled for Brake Pipe Defect

    Piaggio is recalling 2020-2021 Vespa GTS 300 and GTV 300 scooters because improperly galvanized brake pipe terminals can reduce braking efficiency and increase crash risk.

    Product
    VESPA — VESPA GTV 300, GTS 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V616000·2020-10-06

    REV Recalls 2019 Road Rescue Type I Ambulances for Door Latch Defect

    REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V611000·2020-10-05

    Yamaha Recalls YZF-R3, XMAX, and MT-03 Models for Rear Reflector Defect

    Yamaha is recalling specific 2015-2020 motorcycles and scooters because condensation on the rear reflector lens may reduce its effectiveness, increasing crash risk.

    Product
    YAMAHA — YAMAHA YZF-R3, XMAX, MT-03
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V613000·2020-10-05

    Volvo Recalls 2020 VNL Trucks for Window Hinge Defect

    Volvo Trucks North America is recalling 2020 VNL vehicles because window hinges may fail if sleeper windows are open, posing a crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide