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.

21326–21350 of 50426

  • HighFDA (Food)·F-0197-2021·2021-01-13

    Valanga Gourmet Snickerdoodle Cookies Recalled for Undeclared Milk Allergen

    Avalanche Distributing is recalling 1,700 Valanga Gourmet Snickerdoodle Cookies because the label fails to declare milk, a major allergen, despite containing whey.

    Product
    Valanga Gourmet brand Snickerdoodle Cookie with cinnamon sugar on the outside. Each cookie is wrapped and sold individually. Expected shelf life 6 months frozen and 2 months refrigerated. Net wt. 4.4 oz (124g). UPC 814524616004. The Snickerdoodle Cookie label is read in…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0781-2021·2021-01-13

    Medline Thyroid Pack Recall Due to Non-X-Ray Detectable Sponge

    Medline Industries is recalling 40 Thyroid Pack CKHA-LF kits because the cylindrical sponge component is not x-ray detectable. The affected units were distributed only to Canada.

    Product
    Thyroid Pack CKHA-LF, Model DYNJ50352B - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0782-2021·2021-01-13

    Medline Aortic Graft Kits Recalled for Non-Detectable Sponge Component

    Medline Industries is recalling 45 aortic graft kits in Canada because the included sponge is not x-ray detectable.

    Product
    Greffe Aorte-LF (product info is in French); Model DYNJ31877F - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·21068·2021-01-13

    Sea to Summit Recalls Camping Pots Due to Burn and Scald Hazards

    Sea to Summit is recalling Alpha and Sigma camping pots because the nylon latch can disengage, causing the handle to detach and posing burn and scald hazards.

    Product
    Sea to Summit Alpha and Sigma camping pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21066·2021-01-13

    Belkin Recalls Portable Wireless Chargers Due to Fire and Shock Hazards

    Belkin is recalling about 2,280 Portable Wireless Charger + Stand Special Edition units because a manufacturing defect can cause overheating, posing fire and shock risks.

    Product
    Belkin "Portable Wireless Charger + Stand Special Edition"
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0784-2021·2021-01-13

    Accuray TomoTherapy System Recalled for MLC Tickling Error

    Accuray is recalling seven TomoTherapy Treatment Systems because an MLC tickling error may cause the delivered radiation dose to rotate from the planned dose.

    Product
    TomoTherapy Treatment System - Product Usage: used as an integrated system for the planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0768-2021·2021-01-13

    Baxter MiniCap Extended Life PD Transfer Set Recalled for Leak Risk

    Baxter Healthcare is recalling 72,771 units of MiniCap Extended Life PD Transfer Sets due to a potential for no-flow and leaks under the twist clamp.

    Product
    MiniCap Extended Life PD Transfer Set
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0198-2021·2021-01-13

    Country Fresh Party Tray Vegetables Recalled for Undeclared Egg Allergen

    Country Fresh Orlando, LLC is recalling Party Tray Vegetables with Ranch Dip due to undeclared egg. The product was distributed in Florida.

    Product
    Party Tray Vegetables with Ranch Dip, packaged in 40 oz (2.5 LBS) plastic tray with lid, UPC 3825911509.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0780-2021·2021-01-13

    Medline Simple Neck Dissection Kit Recalled for Non-X-Ray Detectable Sponge

    Medline Industries is recalling 90 units of Simple Neck Dissection kits because the cylindrical sponge component is not x-ray detectable.

    Product
    Simple Neck Dissection, Model DYNJ47481C - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0777-2021·2021-01-13

    Boston Scientific Recalls Hot AXIOS Stent Delivery Systems Due to Fitting Detachment

    Boston Scientific is recalling Hot AXIOS Stent delivery systems because a fitting may detach, risking leakage of bodily contents into the peritoneal cavity.

    Product
    Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm (OUS) UPN: M00553550 - Product Usage: The stent is intended for implantation up to 60 days and should be removed upon confirmation of pseudocyst or walled-off necrosis resolution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V005000·2021-01-12

    Smeal Recalls 2020 Aerial and Pumper Vehicles for Remote Controller Defect

    Smeal is recalling 2020 Aerial and Pumper vehicles because a wireless remote controller defect may cause batteries to discharge faster, potentially hindering firefighting efforts.

    Product
    SMEAL — SMEAL AERIAL, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E003000·2021-01-12

    Strategic Sports Recalls Simpson Shorty OTW Motorcycle Helmets

    Strategic Sports is recalling 3,752 Simpson Shorty OTW helmets that lack proper retention and protection, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V002000·2021-01-08

    Marion Body Works Recalls 2018 Freightliner M2 License Plate Light

    Marion Body Works is recalling one 2018 Freightliner M2-106 vehicle because a license plate light may be aimed at other drivers, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21718·2021-01-07

    Noble House Recalls Chests and Cabinets Due to Tip-Over Hazards

    Noble House Home Furnishings is recalling four models of chests, cabinets, and dressers because they are unstable and can tip over, posing serious hazards to children.

    Product
    Chests, cabinets and dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21717·2021-01-07

    John Deere Recalls Frontier Rotary Tillers Due to Injury Hazard

    John Deere is recalling Frontier rotary tillers because some lack a safety sign warning of entanglement hazards. No injuries have been reported.

    Product
    Frontier model rotary tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01072021-01·2021-01-07

    HyVee Chicken Enchiladas Recalled for Undeclared Soy Allergen

    USDA FSIS issued a public health alert for HyVee Chicken Enchiladas due to misbranding and an undeclared soy allergen. Consumers with soy allergies should discard the product.

    Product
    FSIS Issues Public Health Alert for Not-Ready-to-Eat, Heat Treated, Not Fully Cooked Chicken Enchilada Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0741-2021·2021-01-06

    Westmed Elongated Oxygen Mask Recalled for Loose Tube Connection

    Westmed is recalling 3,000 units of the REF 3102-E Elongated Oxygen Mask because the tube connection may become loose, potentially delaying oxygen therapy.

    Product
    REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 - Product Usage: intended to connect with an oxygen source to deliver oxygen therapy to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2021·2021-01-06

    Merit Medical Systems Recalls Custom Embolization Kits Due to Sterility Concerns

    Merit Medical Systems is recalling 42 custom embolization kits because header bags may not be fully sealed, potentially compromising the sterile barrier and leading to infection.

    Product
    Product Code: K12T-02871, Revision A, Custom Procedure Kit, Embolization Kit Sterile EO, Rx Only, (01)00884450339121 For Angiography/angioplasty. The contents of the kit include surgical drapes, towels, medicine cups, needles, various bowls, pen and label sets (PAL)…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0765-2021·2021-01-06

    BD Phoenix PMIC-109 Recalled for False SXT Resistance Results

    Becton Dickinson is recalling BD Phoenix PMIC-109 in vitro diagnostic devices because they may produce false resistant results for S. aureus, potentially affecting antibiotic treatment choices.

    Product
    BD Phoenix" PMIC-109: IVD is intended for the in vitro rapid identification (ID) of gram-positive bacteria from pure culture belonging to the genera Staphylococcus, Enterococcus, and other gram-positive cocci and gram-positive bacilli Catalog Number: 448419
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0183-2021·2021-01-06

    Cipla Recalls Esomeprazole Magnesium Due to Theophylline Contamination

    Cipla is recalling specific lots of Esomeprazole Magnesium delayed-release oral suspension because the excipient Crospovidone is contaminated with theophylline.

    Product
    ESOMEPRAZOLE MAGNESIUM — ESOMEPRAZOLE MAGNESIUM (ESOMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0754-2021·2021-01-06

    Roche cobas 8000 Modular Analyzer Recall for Potential Configuration Errors

    Roche is recalling cobas 8000 modular analyzers because configuration settings may change, causing incorrect results that could go undetected.

    Product
    Roche cobas 8000 modular analyzer series (i.e., cobas 8000 ISE module; cobas c 502, 701, and 702 modules; and cobas e 602 and 801 modules). Chemistry Analyzer (photometric discrete), for clinical use Part Number: 08763662001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0753-2021·2021-01-06

    Intersurgical Smoothbore Breathing System Recalled for Incorrect Exhalation Port

    Intersurgical Inc is recalling 200 Smoothbore breathing systems with exhalation port 22 mm because they were assembled with the incorrect port, which can cause gas leakage.

    Product
    Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Custom Anasthesia Breathing Systems; Multipac Anasthesia Breathing Systems - Product Usage: intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and…
    Category
    Medical Device
    Distribution
    0 states