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.

17251–17275 of 53124

  • HighNHTSA·22V396000·2022-06-06

    Micro Bird Recalls 2017-2018 G5 School Buses Due to Seat Belt Defect

    Micro Bird is recalling 2017-2018 G5 school buses because an incorrect bracket may interfere with the driver's seat belt pretensioner, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V395000·2022-06-06

    Forest River Recalls 2022 Travel Trailers Due to Table Weld Defect

    Forest River is recalling 2022 East to West Alta and Palomino SolAire travel trailers because incomplete welds on the swing-up table base may cause it to drop unexpectedly, increasing injury risk.

    Product
    EAST TO WEST — EAST TO WEST, PALOMINO ALTA, SOLAIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22146·2022-06-02

    Asweets Recalls Wonder & Wise Baby Activity Walkers for Strangulation Hazard

    Asweets is recalling about 13,300 Wonder & Wise baby activity walkers because rubber rings on the rear wheels can detach, posing a strangulation hazard to young children. No injuries have been reported.

    Product
    Wonder & Wise Baby Activity Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22141·2022-06-02

    Communicorp Recalls Aflac Plush Promotional Ducks for Phthalates and Lead

    Communicorp is recalling about 600,000 six-inch Aflac plush promotional ducks distributed to Aflac employees and customers from February 2009 through March 2021. The ducks contain phthalates and lead levels that exceed federal standards and pose a risk if ingested by young children.

    Product
    6" Aflac Plush Promotional Ducks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22145·2022-06-02

    Children's Robes Recalled Due to Burn Hazard

    Joey Clothing is recalling about 15,930 children's robes sold online because they fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V393000·2022-06-02

    Winnebago Recalls 2020 ERA Motorhomes Due to Gas Leak Risk

    Winnebago is recalling 2020 ERA motorhomes because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    WINNEBAGO — WINNEBAGO ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22144·2022-06-02

    Demdaco Microwavable Bowl Holders Recalled for Fire Hazard

    Demdaco microwavable bowl holders can char and catch fire when microwaved for the recommended time. The company received three reports of charring incidents and is offering refunds.

    Product
    Microwavable bowl holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22143·2022-06-02

    Frigidaire and Electrolux Refrigerators Recalled for Ice Maker Choking Hazard

    Electrolux is recalling about 367,500 Frigidaire and Electrolux refrigerators because the ice level detector arm in the ice maker can break apart and fall into the ice bucket, creating a choking hazard.

    Product
    Frigidaire and Electrolux Side-by-Side, Top Freezer and Multi-door refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22142·2022-06-02

    Target Recalls Children's Cat & Jack Unicorn Cozy Pajama Sets for Burn Hazard

    Target is recalling about 120,000 children's pajama sets because they fail to meet federal flammability standards for sleepwear, posing a burn injury risk to children. Consumers should return the pajamas to Target for a full refund.

    Product
    Children's pajama sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0925-2022·2022-06-01

    FDA Recalls Compounded Injectable for Lack of Sterility Assurance

    Olympia Compounding Pharmacy recalls a multi-drug injectable compound (lot B41C22-22) due to inability to assure sterility. The recall affects 1,159 vials distributed nationwide.

    Product
    FA Papaverine 20 mg/mL Phentolamine 2 mg/mL Alprostadil 20 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx Only, 6700 Olympia Pharmaceuticals, Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1084-2022·2022-06-01

    HEB Bakery Cookie Tray Recalled for Potential Metal Fragments

    HEB Bakery Simply Delicious Cookies with Brownie Bites Party Tray (UPC 041220488988, Lot 22063 07:08) is being recalled due to potential metal fragments in the product distributed in Texas.

    Product
    HEB Bakery Simply Delicious Cookies with Brownie Bites Party Tray NET WT 44.24 OZ (2.76 LB) 1.25 kg UPC 041220488988 packaged in a plastic party platter tray with lid
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0943-2022·2022-06-01

    Ondansetron Hydrochloride vials recalled due to sterility assurance concerns

    Olympia Compounding Pharmacy recalls 911 vials of Ondansetron Hydrochloride (1 mg/mL) due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.

    Product
    Ondansetron Hydrochloride, 1 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0127-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V390000·2022-06-01

    Adam Horse Trailer Recall for Damaged Cooktop Burner Valves

    Dalton Enterprises is recalling 2021-2022 Adam J2040 horse trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    ADAM — ADAM HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0945-2022·2022-06-01

    FDA Recalls Phenylephrine 1 mg/mL Vials for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling 9,102 vials of Phenylephrine 1 mg/mL due to lack of assurance of sterility. The affected vials were distributed nationwide in the United States, Puerto Rico, and US Virgin Islands.

    Product
    Phenylephrine 1 mg/mL, Multi-Dose 5 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0021-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0895-2022·2022-06-01

    Blood pressure medication Losartan and hydrochlorothiazide recalled for elevated azido impurity

    Direct Rx recalled Losartan Potassium and Hydrochlorothiazide tablets due to azido impurity levels exceeding acceptable limits. The recall affects 11 bottles distributed in Florida.

    Product
    LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0933-2022·2022-06-01

    Compounded pharmaceutical vials recalled due to sterility assurance failure

    Olympia Compounding Pharmacy is recalling Lipostat-Plus vials nationwide due to lack of sterility assurance. Approximately 4,843 vials were distributed across the USA, Puerto Rico, and US Virgin Islands.

    Product
    Lipostat-Plus Methionine 25 mg/mL Inositol 50 mg/mL Choline Chloride 50 mg/mL Cyanocobalamin 1 mg/mL Pyridoxine HCL 175 mcg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0047-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0905-2022·2022-06-01

    Sodium Selenite Injectable Vials Recalled for Sterility Assurance Failure

    Olympia Compounding Pharmacy recalls 2,333 vials of Sodium Selenite 200 mg/mL injection due to a lack of assurance of sterility. The product was distributed nationwide in the USA, Puerto Rico, and the U.S. Virgin Islands.

    Product
    Sodium Selenite 200 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0074-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1088-2022·2022-06-01

    Mrs. Miller's Homemade Jam Recalled for Undeclared Soy Allergen

    Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam is being recalled because the label does not declare soy allergen. 5,315 cases were distributed across 15 states.

    Product
    Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case
    Category
    Food
    Distribution
    15 states
  • HighFDA (Drugs)·D-0899-2022·2022-06-01

    Compounded Injectable Medication Recalled Due to Sterility Assurance Concerns

    Olympia Compounding Pharmacy recalled 1,710 vials of RE-2 injectable medication due to lack of assurance of sterility. Affected vials were distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.

    Product
    RE-2 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL, Packaged as a) 2.5 mL Multi Dose vial, NDC 73198-0016-03; b) 10 mL Multi Dose vial, NDC 73198-0016-10; Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0935-2022·2022-06-01

    Magnesium Chloride injection recalled due to lack of sterility assurance

    Olympia Compounding Pharmacy is recalling 1,597 vials of Magnesium Chloride injection due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.

    Product
    Magnesium Chloride, 200 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0072-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0900-2022·2022-06-01

    Compounded Injectable Drug Recalled for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling SB-5, a multi-dose injectable medication, due to lack of assurance of sterility. The product was distributed nationwide; patients should contact their healthcare provider immediately.

    Product
    SB-5 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE 50 mcg/mL, Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0024-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0931-2022·2022-06-01

    Lidocaine-Epinephrine Injectable Vials Recalled for Sterility Assurance Failure

    Olympia Compounding Pharmacy is recalling Lidocaine 1%/Epinephrine 1:100,000 injection vials due to lack of sterility assurance. The recall affects 310 vials distributed nationwide.

    Product
    Lidocaine 1%/Epinephrine 1:100,000/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0099-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0927-2022·2022-06-01

    Compounded Injectable Formula F1 Recalled for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling Formula F1, a compounded injectable medication, due to lack of sterility assurance. The 1,703 vials were distributed nationwide.

    Product
    Formula F1 Papaverine 1.8 mg/mL Phentolamine 0.2 mg/mL Alprostadil 18 mcg/mL Atropine 0.02 mg/mL, Packaged as a)2.5 mL Multi-Dose vial, NDC 73198-0001-03; b) 10 mL Multi-Dose vial, NDC 73198-0001-10; Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0941-2022·2022-06-01

    FDA Recalls Olympia Mineral Blend Injectable for Lack of Sterility Assurance

    Olympia Compounding Pharmacy recalls 6,113 vials of Olympia Mineral Blend injectable due to lack of assurance of sterility. The product was distributed nationwide; patients should not use it and should consult their healthcare provider.

    Product
    Olympia Mineral Blend Magnesium Chloride 80 mg/mL Zinc Sulfate 1 mg/mL Manganese Sulfate 20 mcg/mL Copper Gluconate 0.2 mg/mL Sodium Selenite 18 mcg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0061-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0887-2022·2022-06-01

    Losartan HCTZ tablets recalled for manufacturing impurity levels above acceptable limits

    RemedyRepack Inc. is recalling Losartan HCTZ 100/12.5 mg tablets due to elevated AZIDO impurity levels exceeding acceptable manufacturing standards. The recall affects bottles distributed to Florida, South Carolina, and Virginia.

    Product
    Losartan HCTZ 100/12.5 mg, 90 count bottles NDC# 70518-2564-00 Repackaged NDC Original NDC # 68180-0216-09
    Category
    Drug
    Distribution
    3 states