The Recall Desk

Hazard

Storage Temperature Deviation recalls

16 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
16
Critical
0
Severe
0
Most recent
2024-01-03

Of the 16 storage temperature deviation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all storage temperature deviation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–16 of 16

  • HighFDA (Drugs)·D-0202-2024·2024-01-03

    Prescription Inhalation Powder Recalled for Storage Temperature Deviation

    Cardinal Healthcare recalls batch 62002532 of Wixela Inhub inhalation powder nationwide due to CGMP deviations. Products were exposed to temperatures outside labeled storage conditions, potentially affecting product stability.

    Product
    WIXELA INHUB — WIXELA INHUB (FLUTICASONE PROPIONATE AND SALMETEROL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0201-2024·2024-01-03

    Warfarin Sodium Tablets Recalled Due to Temperature Storage Deviation

    Cardinal Healthcare recalls Warfarin Sodium Tablets (5 mg) nationwide due to CGMP deviations: products were exposed to temperatures outside labeled storage conditions, potentially affecting drug stability.

    Product
    WARFARIN SODIUM — WARFARIN SODIUM (WARFARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0181-2024·2024-01-03

    Lansoprazole Suspension Recalled Due to Temperature Storage Deviations

    A prescription lansoprazole suspension has been recalled because batches were exposed to temperatures outside the manufacturer's labeled storage range. This manufacturing quality issue affects Batch 21025A nationwide.

    Product
    FIRST LANSOPRAZOLE PT 3MG/ML, 300ML, Rx Only, Distributed By: CutisPharma, Inc., Woburn, MA 01801. NDC: 65628-080-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0169-2024·2024-01-03

    FDA recalls Asmanex asthma inhalation powder for improper storage conditions

    Cardinal Healthcare is recalling Asmanex Twisthaler inhalers (batch U027458) because they were exposed to temperatures outside their labeled storage conditions. The FDA classified this as a Class II recall due to the manufacturing deviation.

    Product
    ASMANEX — ASMANEX (MOMETASONE FUROATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0162-2024·2024-01-03

    Albuterol sulfate inhalation aerosol recalled for temperature storage deviation

    Cardinal Healthcare recalls albuterol sulfate inhalation aerosol batch MY7E nationwide due to exposure to temperatures outside labeled storage conditions. The precautionary recall affects 2 cartons.

    Product
    ALBUTEROL SULFATE — ALBUTEROL SULFATE (ALBUTEROL SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0804-2023·2023-01-11

    C. difficile diagnostic kit recalled due to storage temperature deviation

    Biomerieux is recalling a C. difficile diagnostic test kit after units were stored outside temperature and time limits, potentially compromising test performance.

    Product
    PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1466-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions

    Colgate Anticavity Fluoride Toothpaste, Optic White Renewal was recalled after being stored outside appropriate temperature conditions. The recall affects 840 packages distributed to Family Dollar stores in 11 states.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITTE RENEWAL, 3% Hydrogen Peroxide, High Impact White, Net Wt. 3.0 OZ. (85 g) UPC 0 35000 97008 4. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1442-2022·2022-08-31

    Mylicon Infant Gas Drops Recalled Due to Temperature Storage Deviation

    Family Dollar Stores is recalling Mylicon Infant Gas Drops 0.5 oz distributed nationwide from April 30 through June 10, 2022 due to improper storage temperature conditions.

    Product
    MYLICON INFANT GAS DROPS 0.5 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1384-2022·2022-08-31

    Family Dollar Hydrocortisone and Cortizone Creams Recalled for Storage Deviation

    Family Dollar Stores is recalling hydrocortisone cream (1 oz, SKU 910321) and Cortizone 10 Creme (0.5 oz, SKU 910167) distributed April 30 through June 10, 2022, due to improper storage temperature conditions.

    Product
    FS HYDROCORTISONE CREAM 1 OZ SKU 910321 CORTIZONE 10 CREME 0.5 OZ SKU 910167 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1447-2022·2022-08-31

    Johnson's Baby First Touch Gift Set Recalled for Storage Temperature Deviations

    Johnson's Baby First Touch Gift Set 4PC is being recalled due to CGMP deviations related to improper storage temperature. The recalled products were distributed nationwide to Family Dollar Store locations between April 30, 2022 and June 10, 2022.

    Product
    JOHNSONS BABY FIRST TOUCH GIFT SET 4PC distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1370-2022·2022-08-31

    Deodorant and Antiperspirant Products Recalled for Temperature Storage Deviations

    Family Dollar Stores is recalling multiple deodorant and antiperspirant products because they were stored outside appropriate temperature conditions. No illnesses or injuries have been reported.

    Product
    SUAVE INV SLD PWDR 1.2 OZ SKU2004504 SUAVE AP INV SOLID SWEET PEA 1.2 OZ SKU 2004622 LADY SPEED STICK AP WILD FREESSIA 1.4OZ SKU 2005184 SUAVE AP DEOD POWDER 2.6 OZ 2PK SKU 2028126 SCRT IN SLD PWDR FRSH 2.1OZ 2PK SKU 2028363 LADY SPD STK AP INV PWDR 1.4OZ SKU 2028365
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1425-2022·2022-08-31

    Family Dollar Laxative Products Recalled for Improper Storage Conditions

    Family Dollar recalls two bisacodyl laxative products (SKUs 902449 and 915221) distributed to specific stores from April to June 2022 due to storage temperature deviations affecting product quality.

    Product
    QP LAXATIVE BISACODYL 5 MG TABLET 50 CT SKU 902449 QP WOMEN LAXATIVE BISCODYL TABLET 25 CT SKU 915221 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1438-2022·2022-08-31

    Carmex Lip Balm Products Recalled Due to Improper Storage Temperatures

    Family Dollar Stores is recalling Carmex lip balm products (three SKUs) distributed from April 30 to June 10, 2022, due to CGMP deviations involving improper storage temperature conditions.

    Product
    CARMEX DAILY CARE CHERRY SPF 15 0.35 OZ SKU 901842 CARMEX LIP BALM JAR 0.25OZ SKU 903284 CARMEX STRWBRRY STCK W SPF 15 0.15OZ SKU 905760 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1403-2022·2022-08-31

    MY CHOICE Levonorgestrel Tablets Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling MY CHOICE Levonorgestrel Tablets due to storage temperature deviations that may affect product efficacy. The tablets were distributed nationwide between April 30 and June 10, 2022.

    Product
    MY CHOICE LEVONORGESTREL TABLET distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1366-2022·2022-08-31

    Personal Care Lotions Recalled Due to Improper Storage Temperature

    Family Dollar Stores is recalling multiple lotion products that were held outside appropriate storage temperatures. The affected brands include Dermasil, Aveeno, and Vaseline products distributed from April 30 through June 10, 2022.

    Product
    Dermasil Dry Skin Treatment 10 OZ SKU 2098068 Aveeno Daily Moisturizing Lotion 5 OZ SKU 2005444 Aveeno Baby Daily Moistue Lotion 8 OZ SKU 900016 Vaseline Mens Extra Strength Body and Face Lotion 10 OZ SKU 2003674 distributed to specific Family Dollar Stores 04/30/2022 thro
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1415-2022·2022-08-31

    Alka Seltzer Extra Strength 24 CT Recalled for Improper Storage Conditions

    Family Dollar Stores is recalling Alka Seltzer Extra Strength 24 CT due to products stored outside proper temperature conditions, which may affect product quality.

    Product
    ALKA SELTZER EXTRA STRENGTH 24 CT distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
    Category
    Drug
    Distribution
    Distributed nationwide