The Recall Desk

Hazard

Improper Storage recalls

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

What the numbers show

Total
226
Critical
0
Severe
1
Most recent
2026-06-24

Of the 226 improper storage recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (0%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all improper storage 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.

176–200 of 226

  • ModerateFDA (Drugs)·D-1323-2022·2022-08-17

    FDA Recalls Dakin's Solution Due to Storage Condition Deviations

    McKesson Medical-Surgical recalled 113 bottles of Dakin's Solution (sodium hypochlorite) nationwide due to improper storage outside label specifications. Products may have compromised stability.

    Product
    DAKINS QUARTER — DAKINS QUARTER (SODIUM HYPOCHLORITE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1319-2022·2022-08-17

    FDA Recalls Miralax Osmotic Laxative Powder for Storage Deviations

    The FDA recalled 67 bottles of Miralax laxative powder due to storage conditions that violated drug label specifications. The precautionary recall is due to potential product quality concerns from improper storage conditions.

    Product
    MIRALAX — MIRALAX (POLYETHYLENE GLYCOL 3350)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1321-2022·2022-08-17

    FDA Recalls Pataday Eye Allergy Drops Due to Storage Deviations

    Mckesson Medical-Surgical is recalling Pataday Once Daily Relief eye drops nationwide because the products were stored outside label specifications. No illnesses have been reported.

    Product
    PATADAY ONCE DAILY RELIEF — PATADAY ONCE DAILY RELIEF (OLOPATADINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1325-2022·2022-08-17

    Racepinephrine Inhalation Solution Recalled for Improper Storage Conditions

    Mckesson Medical-Surgical is recalling S2 Racepinephrine Inhalation Solution due to storage that deviated from label specifications. This Class II recall affects 23 cartons distributed nationwide.

    Product
    S2 — S2 (RACEPINEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1322-2022·2022-08-17

    FDA Recalls A&D Original Ointment due to improper storage conditions

    A&D Original Ointment 16 oz jars are being recalled nationwide because products were stored outside manufacturer specifications. The recall affects all NDC 11523-0096-3 units distributed in the USA.

    Product
    A&D Original Ointment, Diaper Rash Ointment & Skin Protectant, 16 oz. Jar, Bayer Healthcare Pharmaceutica, NDC 11523-0096-3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0976-2022·2022-06-08

    AMBI Skincare Fade Cream Recalled for Temperature Storage Deviations

    AMBI Skincare Fade Cream is being recalled nationwide due to cGMP violations. The product was stored outside its labeled temperature requirements during manufacturing.

    Product
    AMBI Skincare Fade Cream Normal Skin, Net Wt. 2 OZ. (56g)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0981-2022·2022-06-08

    Aveeno Daily Moisturizing Lotion recalled due to improper storage conditions

    Family Dollar and Johnson & Johnson Consumer are recalling Aveeno Daily Moisturizing Lotion due to cGMP violations involving improper storage temperature. No illnesses have been reported.

    Product
    Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0977-2022·2022-06-08

    AMBI Skincare Fade Cream Recalled for Improper Temperature Storage

    AMBI Skincare Fade Cream Oily Skin (2 OZ) is recalled nationwide due to improper storage temperature. The product was stored outside the temperature requirements specified on its label.

    Product
    AMBI Skincare Fade Cream Oily Skin New & Improved, Net Wt. 2 OZ (56g)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0980-2022·2022-06-08

    Hand Sanitizer Recall: Storage Temperature Non-Compliance at Family Dollar

    Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer Moisturizing Formula due to cGMP deviations related to improper storage outside labeled temperature requirements.

    Product
    Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96536 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1140-2022·2022-06-01

    Medical Calcium Reagent Shipped Without Required Refrigeration; QC Failure Risk

    A medical lab reagent (ABX Pentra Calcium AS CP) was shipped at room temperature instead of refrigerated, causing probable quality control failure. Affected patients may experience diagnostic delays and require repeat testing.

    Product
    ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Drugs)·D-0883-2022·2022-05-25

    Trulicity Injection Recalled Due to Temperature Exposure During Shipment

    A batch of Trulicity (dulaglutide) injection was recalled due to temperature exposure during distribution in New Mexico. The product was exposed to temperatures outside its labeled storage requirements due to inclement weather.

    Product
    Trulicity (dulaglutide) injection, 1.5 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 00002-1434-80
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0932-2022·2022-04-20

    Hydroxybutyrate Test Kits Recalled Due to Improper Storage

    Medline's Hydroxybutyrate LiquiColor Tests are recalled due to improper storage that may cause delayed test results. The recall affects 45 units distributed across 16 U.S. states.

    Product
    Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0933-2022·2022-04-20

    Medical Device Linearity Standards Recalled Due to Improper Storage Controls

    Medline Industries is recalling Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards due to improper storage controls that may affect test result timing. The recall affects 10 boxes distributed to healthcare facilities in six states.

    Product
    Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-604, Medline catalog number S-O2450604, IVD.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0656-2022·2022-03-02

    Medline Michels Transport Medium Recalled for Improper Storage Conditions

    Medline is recalling 2,816 Michels Transport Medium prefilled containers due to improper storage in a temperature-controlled setting instead of refrigeration.

    Product
    Michels Transport Medium, 20ML Prefilled Cont
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0678-2022·2022-03-02

    ImmunoCard STAT Rotavirus diagnostic tests recalled for improper storage temperature

    Meridian BioscienceImmunoCard STAT! Rotavirus tests were shipped at room temperature instead of refrigerated, which may affect their reliability.

    Product
    meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immunoassay is a rapid in vitro qualitative procedure for the detection of rotavirus antigen in human stool. The test can be used to aid in the diagnosis of rotaviru
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Food)·F-0632-2022·2022-02-16

    Natural Way Cheese Chive Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese Chive Cheese Curds (12oz bags) distributed in Michigan and Indiana are recalled because milk used was stored beyond the required 72-hour tank cleaning interval, creating a risk of bacterial growth.

    Product
    Natural Way Cheese Chive Cheese Curds, retail 12oz plastic bag UPC 8 10056 75107 4, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0636-2022·2022-02-16

    Natural Way Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese White Cheddar Cheese Curds are being recalled because milk used in the product exceeded the required 72-hour tank cleaning interval. Consumers should not consume this product.

    Product
    Natural Way Cheese White Cheddar Cheese Curds, retail 12oz plastic bag UPC 8 10056 75021 3, 12 retail units per wholesale case, and sold in 10lbs wholesale plastic bag as well
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0641-2022·2022-02-16

    Natural Way Cheese Sweet Basil Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese is recalling Sweet Basil Cheese Curds because the milk used was stored in a holding tank for more than 72 hours, exceeding required cleaning intervals.

    Product
    Natural Way Cheese Sweet Basil Cheese Curds, retail 12oz plastic bag UPC 8 10056 75015 2, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0637-2022·2022-02-16

    Natural Way Cheese 3 Pepper Cheese Curds recalled for improper milk storage

    Natural Way Cheese is recalling 3 Pepper Cheese Curds (12oz bags) distributed in Michigan and Indiana due to milk stored in a holding tank for more than 72 hours, exceeding required cleaning intervals.

    Product
    Natural Way Cheese 3 Pepper Cheese Curds, retail 12oz plastic bag UPC 8 10056 75020 6, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0638-2022·2022-02-16

    Natural Way Cheese Bacon Cheddar Cheese Curds recalled for improper storage

    Natural Way Cheese Bacon Cheddar Cheese Curds are being recalled in Michigan and Indiana because milk used in production was stored in a holding tank exceeding the required 72-hour cleaning interval.

    Product
    Natural Way Cheese Bacon Cheddar Cheese Curds, retail 12oz plastic bag UPC 8 10056 75175 3, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0642-2022·2022-02-16

    Natural Way Cheese Cheddar Curds recalled for improper milk storage

    Natural Way Cheese is recalling Cheddar Cheese Curds because milk used in production was stored in a holding tank for longer than the required 72-hour cleaning interval, creating potential for contamination.

    Product
    Natural Way Cheese Cheddar Cheese Curds, retail 12oz plastic bag UPC 8 10056 75023 7, 12 retail units per wholesale case, and sold in 10lbs wholesale plastic bag as well
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0640-2022·2022-02-16

    Natural Way Cheese Dill Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese is recalling Dill Cheese Curds because milk was stored in a holding tank longer than the required 72-hour cleaning interval. The improper storage creates a potential food safety risk.

    Product
    Natural Way Cheese Dill Cheese Curds, retail 12oz plastic bag UPC 8 10056 75019 0, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0633-2022·2022-02-16

    Cheese Curds Recalled for Improper Milk Storage in Michigan and Indiana

    Natural Way Cheese Marble Cheese Curds are being recalled because the milk used was stored beyond the required 72-hour tank cleaning interval, creating potential food safety risk.

    Product
    Natural Way Cheese Marble Cheese Curds, retail 12oz plastic bag UPC 8 10056 75022 0, 12 retail units per wholesale case, and sold in 10lbs wholesale plastic bag as well
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0552-2022·2022-02-09

    Premier Rotaclone Medical Device Recalled Due to Improper Storage Conditions

    Medline Industries is recalling 34 units of the Premier Rotaclone (Lot 696004N116) due to improper storage in temperature-controlled settings instead of required refrigeration. This may affect device performance or safety.

    Product
    Premier Rotaclone, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2022·2021-12-29

    Stanbio TDM/B-Hydroxybutyrate Controls Recalled Due to Improper Storage Temperature

    Medline Industries is recalling Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls due to improper storage conditions. The product was shipped at room temperature instead of the required refrigerated environment.

    Product
    Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
    Category
    Medical Device
    Distribution
    Distributed nationwide