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 the agency’s own highest classification or reported deaths or serious injuries, 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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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

23576–23600 of 90106

  • HighFDA (Drugs)·D-1486-2022·2022-09-14

    Acetaminophen Oral Solution Recalled for Manufacturing Process Control Failures

    Plastikon Healthcare LLC is recalling acetaminophen oral solution (650 mg per 20.3 mL cup) distributed nationwide due to manufacturing process control failures.

    Product
    Acetaminophen Oral Solution 650 mg / 20.3 mL, 20.3 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6820-76
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V687000·2022-09-14

    2022 Volkswagen Taos Engine Stall Software Safety Recall

    Volkswagen is recalling certain 2022 Taos vehicles with all-wheel drive due to engine control unit software that may cause engine stall when coming to a stop, increasing crash risk. Dealers will provide free software updates.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1709-2022·2022-09-14

    Piantedosi Burger Rolls Recalled for Cronobacter and Botulinum Contamination

    Piantedosi Baking Co. is recalling frozen Gourmet Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 units across 15 states.

    Product
    Gourmet Burger Roll 12-pack (033474501322)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1722-2022·2022-09-14

    Brioche-Style Slider Rolls Recalled Due to Bacterial Contamination Risk

    Piantedosi Baking Co. is recalling 18,119 frozen Brioche-Style Slider Roll 24-packs distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche-Style Slider Roll 24-pack (033474512021)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1677-2022·2022-09-14

    CARTO VIZIGO Guiding Sheath Recalled Due to Water-Damaged Sterile Packaging

    Biosense Webster is recalling 98 units of CARTO VIZIGO 8.5F guiding sheaths due to water damage to packaging that may have compromised the sterile barrier, creating a potential infection risk.

    Product
    CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into the heart.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1692-2022·2022-09-14

    Banana Nut Pound Cake Recalled Due to Undeclared Soy Allergen

    Select Bakery Gourmet Banana Nut Pound Cake contains undeclared soy, posing a risk to consumers with soy allergies. The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Gourmet Banana Nut Pound Cake Net Wt. 3oz (85g) & 5 oz (142g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10058 2
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1685-2022·2022-09-14

    MEGA Intra-Aortic Balloon Catheter Recalled for Undersized Dilator

    Datascope Corporation is recalling 10,427 units of the MEGA 8Fr 50cc Intra-Aortic Balloon Catheter due to an undersized dilator in certain lots. The device has been distributed internationally and is awaiting domestic distribution.

    Product
    MEGA 8Fr 50cc Intra-Aortic Balloon Catheter
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1717-2022·2022-09-14

    Frozen Brioche Burger Rolls Recalled for Bacterial Contamination

    Piantedosi Baking Co. is recalling Brioche Style Burger Rolls (UPC 033474504170) distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Brioche Style Burger Roll 12-pack (033474504170)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1490-2022·2022-09-14

    Guaifenesin and dextromethorphan liquid medication recalled for manufacturing control issues

    Plastikon Healthcare LLC is recalling guaifenesin and dextromethorphan liquid medication (280,500 cups) distributed nationwide due to manufacturing control deviations in production.

    Product
    GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1701-2022·2022-09-14

    Obstetric and gynecology surgical packs recalled for unvalidated sterilization exposure

    American Contract Systems is recalling 15 obstetric and gynecology surgical packs that underwent multiple sterilization cycles without validation. This could compromise product sterility and increase infection risk during procedures.

    Product
    Various ob/gyn packs
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Drugs)·D-1492-2022·2022-09-14

    CORRECTDOSE Children's Allergy Relief Recalled Due to Manufacturing Process Control Deviations

    CORRECTDOSE Children's Allergy Relief (Diphenhydramine HCl 12.5 mg per 5 mL) is being recalled nationwide. The FDA determined products were manufactured under conditions with inadequate process control.

    Product
    CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL), 2.04 FL. OZ (60 mL) packaged in 12- 5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-302-05 UPC 8 60003 67144 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1703-2022·2022-09-14

    Select Bakery Peanut Butter Delight recalled for undeclared soy and Red #40

    Select Bakery Peanut Butter DELIGHT (3 oz packages) is recalled because it contains undeclared soy and Red #40. The product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Peanut Butter DELIGHT Net Wt. 3 Oz (85g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10028 5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-1484-2022·2022-09-14

    Acetaminophen Oral Solution 160 mg Recalled for Manufacturing Control Deviations

    Acetaminophen Oral Solution 160 mg/5 mL (290,270 cups) recalled nationwide due to CGMP manufacturing control deviations. Product was distributed to institutional healthcare facilities.

    Product
    Acetaminophen Oral Solution 160 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152, NDC 0904-6738-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2022·2022-09-14

    Early Bird Bleed Monitoring System Introducer fails to power on

    Saranas, Inc. is recalling 953 units of the Early Bird Bleed Monitoring System Introducer Sheath Set due to a design error that prevents the device from powering on and completing self-tests. The product was distributed nationwide.

    Product
    Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1488-2022·2022-09-14

    Diphenhydramine Solution Recalled Due to Manufacturing Control Deviations

    Plastikon Healthcare LLC is recalling Diphenhydramine HCl Oral Solution nationwide due to manufacturing control deficiencies that did not meet Current Good Manufacturing Practice standards.

    Product
    Diphenhydramine HCl Oral Solution 12.5 mg / 5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6740-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1706-2022·2022-09-14

    Frozen Finger Rolls Recalled Due to Potential Bacterial Contamination

    Piantedosi Baking Co. is recalling 18,119 trays of frozen finger rolls distributed across 15 states due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.

    Product
    Finger Roll 24-pack (033474400885))
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-1487-2022·2022-09-14

    Calcium Carbonate Oral Suspension Recalled Due to Manufacturing Control Deviations

    Plastikon Healthcare recalls 49,280 cups of Calcium Carbonate Oral Suspension (1250 mg/5 mL) distributed nationwide due to manufacturing process control failures during production.

    Product
    CALCIUM CARBONATE ORAL SUSPENSION, 1250 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 4 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-7098-94
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1719-2022·2022-09-14

    B & W frozen burger rolls recalled for contamination risk

    B & W Gourmet Burger Rolls are being recalled due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products were distributed across 15 states.

    Product
    B & W Gourmet Burger Roll 12-pack (033474504644)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1716-2022·2022-09-14

    Split Top Burger Rolls recalled for possible bacterial contamination

    Piantedosi Baking Co. is recalling Split Top Burger Rolls due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected products were distributed across multiple northeastern and southeastern states.

    Product
    Split Top Burger Roll 12-pack (033474503777)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1693-2022·2022-09-14

    Blueberry Pound Cake Recalled for Undeclared Soy and Food Colorings

    Select Bakery Gourmet Blueberry Pound Cake (5 oz) is recalled due to undeclared soy and food colorings. The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Gourmet Blueberry Pound Cake Net Wt. 5 Oz (142g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10060 5
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1661-2022·2022-09-14

    Handheld ultraviolet-C germicidal wand recalled for excessive radiation

    MERCHSOURCE LLC is recalling a handheld ultraviolet-C germicidal wand (model 1013622) due to excessive ultraviolet-C radiation emission. Consumers should stop using the product immediately.

    Product
    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1702-2022·2022-09-14

    Hysterectomy and Vaginal Packs Recalled for Improper Sterilization Validation

    American Contract Systems recalled 29 hysterectomy and vaginal packs distributed to health systems in 13 states due to exposure to multiple sterilization cycles without validation.

    Product
    Various hysterectomy, vaginal packs
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Food)·F-1720-2022·2022-09-14

    Piantedosi Slider Rolls No Seeds frozen product recall for bacterial contamination

    Piantedosi Baking Co. is recalling Slider Rolls No Seeds 24-pack due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. The recall affects 18,119 units distributed across 15 states.

    Product
    Slider Rolls No Seeds 24-pack (033474504941)
    Category
    Food
    Distribution
    15 states
  • HighFDA (Food)·F-1695-2022·2022-09-14

    Select Bakery pound cake recalled for undeclared soy and food dyes

    Select Bakery Gourmet Old Fashion Pound Cake (5 oz) is being recalled due to undeclared soy allergen and artificial food dyes (Yellow #5, Yellow #6, Red #40). The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    Select Bakery Gourmet Old Fashion Pound Cake Net Wt. 5 Oz (142g) Select Bakery, Inc., Rockwell, N.C. 28138 UPC 0 28598 10062 9
    Category
    Food
    Distribution
    3 states