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.

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 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.

51–75 of 226

HighFDA (Drugs)·D-0566-2023·2023-05-10
Advil Liqui-Gels 200 mg ibuprofen capsules recalled for improper storage
Family Dollar Stores is recalling Advil Liqui-Gels 200 mg ibuprofen capsules (SKUs 0999841 and 0916071) distributed nationwide due to storage outside labeled temperature requirements.
Product
Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0564-2023·2023-05-10
Advil Ibuprofen 200mg tablets recalled due to improper storage conditions
Family Dollar Stores is recalling Advil Ibuprofen 200mg caplets stored outside temperature requirements. The recall affects units distributed nationwide from July 2022 through March 2023.
Product
Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0778-2023·2023-05-10
Sofrito Marinating Sauce recalled for improper storage conditions
20-100 Delicious Seasoning LLC recalls Sofrito Marinating Sauce because the product was not stored refrigerated as required. Consumers should not consume the product.
Product
Sofrito Marinating Sauce, 100% All Natural Ingredients (Caribbean Seasoning), Net Wt 16 oz. (460g), 8 oz. (230g) and 32(920g) oz. Glass Jar. Manufactured and Distributed by 20100 Seasoning LLC. Keep Refrigerated.
Category
Food
Distribution
0 states
ModerateFDA (Drugs)·D-0565-2023·2023-05-10
Advil Dual Action Pain Reliever Recalled for Storage Temperature Deviation
Family Dollar Stores is recalling Advil Dual Action pain reliever tablets (36-caplet bottles, SKU 0902867) nationwide because the product was stored outside labeled temperature requirements.
Product
Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0563-2023·2023-05-10
Advil Ibuprofen Tablets Recalled for Storage Temperature Deviation
Family Dollar Stores is recalling Advil Ibuprofen 200 mg tablets due to a storage temperature deviation during manufacturing and distribution. No illnesses have been reported.
Product
Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2023·2023-01-11
API 20 C AUX Diagnostic Strips Recalled Due to Storage Temperature Exceedance
Biomerieux Inc is recalling API 20 C AUX diagnostic strips due to storage conditions that exceeded temperature and time specifications. The manufacturer cannot guarantee product performance.
Product
API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2023·2023-01-11
Medical Device Reagent Recall Due to Storage Condition Exceedance
Biomerieux is recalling DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 reagent kits because temperature and time storage conditions were exceeded, preventing performance guarantees. Distributed nationwide, affected units should be removed from service.
Product
DCOUNT SYSTEMS REAGENTS CHEMCHROME V14 (6X1.8ML), CATALOG 306-R1026-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0830-2023·2023-01-11
ETEST Tobramycin Susceptibility Test Recalled for Storage Condition Failure
Biomerieux is recalling ETEST Clinical Tobramycin susceptibility test strips (batch 1009434160) because temperature and storage time conditions were exceeded during distribution. Product performance cannot be guaranteed due to these storage failures.
Product
ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0783-2023·2023-01-11
Listeria Detection Test Strips Recalled for Unreliable Performance
Biomerieux is recalling API Listeria detection test strips that were exposed to temperature and time exceedance during storage. Product performance cannot be guaranteed as a result.
Product
API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0826-2023·2023-01-11
Levofloxacin ETEST Clinical Test Recalled for Improper Storage Conditions
Biomerieux Inc. is recalling 7 units of ETEST CLINICAL LEVOFLOXACIN LE 32 US S30 diagnostic test kits (Batch 1009240000) due to temperature and time storage condition violations that prevent guarantee of product performance.
Product
ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0864-2023·2023-01-11
VIDAS HCG 60 Clinical Test Kits Recalled for Exceeded Storage Conditions
Biomerieux Inc is recalling VIDAS HCG 60 test kits because storage conditions were exceeded, which cannot guarantee product performance. No illnesses or injuries have been reported.
Product
VIDAS CLINICAL VIDAS HCG 60 TESTS, CATALOG 30405-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0805-2023·2023-01-11
Bioball Fungal Reference Standard Recalled for Temperature Storage Issues
Biomerieux Inc. recalled 2 units of BIOBALL A.BRASILIENSIS NCPF 2275 reference standard (Batch 7112) after temperature and time storage conditions exceeded acceptable ranges. The manufacturer cannot guarantee product performance.
Product
BIOBALL A.BRASILIENSIS NCPF 2275 550X20, CATALOG 56011
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0839-2023·2023-01-11
Biomerieux CHROMID CARBA Laboratory Product Recalled Due to Storage Condition Violations
Biomerieux Inc is recalling CHROMID CARBA laboratory products nationwide because storage conditions exceeded acceptable temperature and time ranges. The company cannot guarantee product performance.
Product
PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT, CATALOG 414012
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1468-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions
Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1642-2022·2022-09-07
T-Cell Xtend Test Kit Recalled Due to Improper Storage Temperature
Oxford Immunotec is recalling 47 units of the T-Cell Xtend REF TTK.610 US test kit due to equipment failure that caused improper storage temperatures outside the validated range. Affected devices may have been compromised.
Product
T-Cell Xtend REF TTK.610 US
Category
Medical Device
Distribution
7 states
HighFDA (Drugs)·D-1465-2022·2022-09-07
Colgate OPTIC WHITE PRO Series Toothpaste Recalled for Improper Storage
Family Dollar Stores is recalling 1,120 packages of Colgate OPTIC WHITE PRO SERIES toothpaste due to improper temperature storage conditions that deviate from cGMP standards.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1470-2022·2022-09-07
Colgate OPTIC WHITE Mouthwash Recalled Due to Improper Storage Conditions
Family Dollar is recalling Colgate Whitening Mouthwash OPTIC WHITE ICY FRESH MINT due to temperature storage deviations. 840 packages were distributed to Family Dollar stores in multiple states.
Product
Colgate Whitening Mouthwash, OPTIC WHITE ICY FRESH MINT. 16 fl. OZ. (1 pt) 473 mL UPC 0 35000 67111 0. Dist. by: Colgate-Palmolive Co. New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1469-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste Recalled Due to Improper Storage Conditions
Family Dollar Stores recalls 1,400 packages of Colgate Anticavity Fluoride Toothpaste due to improper temperature storage conditions during manufacturing. The product may not meet quality standards.
Product
Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT PASTE. Net Wt. 4.2 OZ. (119 g) UPC 0 35000 45836 0. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1467-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions
Colgate Anticavity Fluoride Toothpaste OPTIC WHITE ADVANCED ICY FRESH is recalled due to improper temperature storage during manufacturing. Approximately 1,680 packages distributed across 11 U.S. states are affected.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY FRESH, Net Wt. 3.2 OZ. (90 g) UPC 0 35000 97159 3. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1402-2022·2022-08-31
Petroleum Jelly Products Recalled for Improper Storage Conditions
Family Dollar Stores is recalling three petroleum jelly products (Swan, Baby Love, and Vaseline brands) distributed between April and June 2022 due to storage temperature deviations.
Product
SWAN PETROLEUM JELLY 7.5 OZ SKU 910721 BABY LOVE PETROLEUM JELLY 13 OZ SKU 910726 VASELINE PETROLEUM JELLY ORIGINAL 7.5 OZ 2099273 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1372-2022·2022-08-31
Tylenol and Acetaminophen Products Recalled Due to Improper Storage
Family Dollar Stores is recalling multiple Tylenol and acetaminophen products due to CGMP deviations involving improper storage temperature conditions. Products were distributed nationwide through specific Family Dollar locations from April 30, 2022 through June 10, 2022.
Product
Ready in case ACETAMINOPHEN PM CAPLETS 24 CT SKU 900559; TYLENOL CHILD GRAPE 4 FL OZ SKU 901600 TYLENOL CHILD ORAL SUSPENSION CHERRY 4 FO 913104 TYLENOL INFANTS DROPS DF CHERRY 1OZ SKU 999108 TYLENOL PM CAPLET 24 CT SKU 900603 TYLENOL EXTRA STRENGTH CAPLET 24 CT SKU 91698
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1426-2022·2022-08-31
GC Milk of Magnesia Recalled for Storage Temperature Deviation
GC Milk of Magnesia products (Cherry and Mint, 12 fl oz) distributed to Family Dollar Stores have been recalled due to improper storage temperature. The products may not meet quality and performance standards.
Product
GC MILK OF MAGNESIA CHERRY 12 FL OZ SKU 915000 GC MILK OF MAGNESIA MINT 12 FL OZ SKU 915623 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1388-2022·2022-08-31
Arthritis Pain Reliefs Recalled for Improper Storage Temperature Conditions
Family Dollar Stores is recalling BC Arthritis Pain Fast Pain Relief and Good Sense Arthritis Caplet due to improper storage conditions. Products were distributed nationwide from April 30 through June 10, 2022.
Product
BC ARTHRITIS PAIN FAST PAIN RELIEF 24CT SKU 999839 GOOD SENSE ARTHRITIS CAPLET 24 CT SKU 914771 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1374-2022·2022-08-31
Antifungal Cream Recalled for Improper Storage Temperature Conditions
Family Dollar's FS Clotrimazole Anti Fungal Cream is being recalled due to improper storage temperature conditions. The product was distributed nationwide between April 30 and June 10, 2022.
Product
FS CLOTRIMAZOLE ANTI FUNGAL CREAM .5 OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1443-2022·2022-08-31
Good Sense Lice Shampoo Recalled for Improper Storage Conditions
Family Dollar Stores recalls Good Sense Lice Shampoo 6 FL OZ distributed April-June 2022 nationwide due to CGMP deviations from improper storage temperature conditions. Products may have compromised safety or efficacy.
Product
GOOD SENSE LICE SHAMPOO 6FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Category
Drug
Distribution
Distributed nationwide