Hazard

Temperature Excursion recalls

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

What the numbers show

Total: 289
Critical: 0
Severe: 4
Most recent: 2025-09-24

Of the 289 temperature excursion recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (1%) 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 temperature excursion 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.

276–289 of 289

ModerateFDA (Drugs)·D-0546-2021·2021-06-02
Cardinal Health Recalls Fexofenadine Tablets Due to Temperature Excursions
Cardinal Health is recalling 321 bottles of Fexofenadine Hydrochloride 180 mg tablets due to intermittent temperature excursions during storage. The affected product was distributed in Florida, Georgia, and South Carolina.
Product
Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine Non-Drowsy 100 Tablets 180 mg Each NDC 45802-571-78 Distributed By Perrigo Allegan, MI 49010
Category
Drug
Distribution
3 states
ModerateFDA (Food)·F-0803-2019·2019-02-13
Wisconsin Cheese Group Recalls Mimoso Queijo Minas Fresco Farmer's Cheese
Wisconsin Cheese Group is recalling Mimoso Queijo Minas Fresco Farmer's Cheese because it was transported at elevated temperatures.
Product
Mimoso Queijo Minas Fresco Farmer's Cheese. Net Wt. 12 oz (340g) UPC 19753-00052 Keep Refrigerated.
Category
Food
Distribution
2 states
ModerateFDA (Devices)·Z-2164-2018·2018-06-20
BioMérieux Recalls VITEK 2 Gram-Positive Cards Due to Temperature Excursion
BioMérieux is recalling VITEK 2 Gram-Positive identification cards in Guadeloupe because a shipment experienced a temperature excursion exceeding acceptable limits.
Product
The VITEK 2 Gram-Positive identification card (GP) is intended for use with the VITEK 2 Systems for the automated identification of most significant Gram-positive organisms. The VITEK 2 GP identification card Is a single-use disposable. GP TEST KIT VTK2 20 CARTES A microorga
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2168-2018·2018-06-20
BioMérieux Recalls VITEK 2 Gram Negative Susceptibility Cards Due to Temperature Excursion
BioMérieux is recalling VITEK 2 Gram Negative Susceptibility Cards shipped to Guadeloupe that experienced a temperature excursion exceeding acceptable limits.
Product
The VITEK 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of clinically significant aerobic gram negative bacilli to antimicrobial agents. Fully automated short-term
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2172-2018·2018-06-20
BioMérieux Recalls Oxidase Reagent Due to Temperature Excursion in Guadeloupe
BioMérieux is recalling Oxidase Reagent (ref: 55635) in Guadeloupe after a shipment experienced temperature excursions up to 47.8°C, exceeding acceptable limits.
Product
Oxidase Reagent (ref: 55635): This test is used to detect the production of the enzyme cytochrome oxidase by bacteria. This enzyme is characteristic of the genus Neisseria and most species of Pseudomonas. It enables the differentiation of Gram (-) bacilli (1, 2). A microorgan
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2170-2018·2018-06-20
BioMérieux PREVI Color Gram Reagents Recalled Due to Temperature Excursion
BioMérieux is recalling PREVI Color Gram reagents shipped to Guadeloupe that experienced a temperature excursion exceeding acceptable limits.
Product
The PREVI¿ Color Gram dyes are used with the PREVI¿ Color Gram instrument to stain bacterial and fungal microorganisms for direct examination, according to Gram s method. The PREVI¿ Color Gram instrument sprays the PREVI¿ Color Gram reagents onto microscope slides which have b
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2171-2018·2018-06-20
BioMérieux Recalls Color Gram 2 Stains Due to Temperature Excursion
BioMérieux is recalling Color Gram 2 stains in Guadeloupe after a shipment experienced a temperature excursion exceeding acceptable limits.
Product
Color Gram 2 (COLOR GRAM 2 - F), these stains are used to stain bacterial and fungal microorganisms for direct examination, according to the Gram method. Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in sol
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2169-2018·2018-06-20
BioMérieux Recalls VIDAS TOXO IgG Avidity Test Due to Temperature Excursion
BioMérieux is recalling VIDAS TOXO IgG Avidity tests because a shipment to Guadeloupe exceeded temperature limits. The products were delivered to customers despite quarantine instructions.
Product
VIDAS TOXO IgG Avidity is an automated qualitative test for use on the VIDAS family instruments, for the determination of anti-toxoplasma IgG avidity in human serum or plasma (lithium heparin, sodium citrate, EDTA) using the ELFA technique (Enzyme Linked Fluorescent Assay). T
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2167-2018·2018-06-20
BioMérieux Recalls VITEK 2 Gram Positive Susceptibility Cards Due to Temperature Excursion
BioMérieux is recalling VITEK 2 Gram Positive Susceptibility Cards in Guadeloupe because a shipment experienced a temperature excursion up to 47.8°C, exceeding acceptable limits.
Product
The VITEK¿ 2 Gram Positive Susceptibility Card is intended for use with the VITEK 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae to antimicrobial agents. Fully automated short
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2166-2018·2018-06-20
BioMerieux VITEK 2 ANC Card Recalled Due to Temperature Excursion
BioMerieux is recalling VITEK 2 ANC identification cards shipped to Guadeloupe that experienced a temperature excursion exceeding acceptable limits.
Product
The VITEK¿ 2 Anaerobic and Corynebacteria identification card (ANC) is intended for use with the VITEK¿ 2 Systems for the automated identification of most clinically significant anaerobic organisms and Corynebatcerium species. The VITEK¿ 2 ANC identification card is a single-use
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-2165-2018·2018-06-20
BioMérieux Recalls VITEK 2 NH Cards Due to Temperature Excursion
BioMérieux is recalling VITEK 2 Neisseria-Haemophilus identification cards in Guadeloupe that were exposed to temperatures exceeding acceptable limits.
Product
The VITEK 2 Neisseria-Haemophilus identification card (NH) is intended for use with the VITEK 2 Systems for the automated identification of most clinically significant fastidious organisms. The VITEK 2 NH identification card is a single-use disposable. A microorganism differe
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-3124-2017·2017-09-20
Leica Biosystems Recalls Napsin A Antibody Due to Temperature Excursion
Leica Biosystems Richmond Inc. is recalling 33 units of Napsin A (MRQ-60 Mab.) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.
Product
Cell Marque, Napsin A (MRQ-60 Mab.), 7 mL, REF PA0805, IVD, The antibody is intended for in vitro diagnostic (IVD) use. Napsin A (MRQ-60) Mouse Monoclonal Primary Antibody is intended for laboratory use in the detection of the Napsin A protein in formalin-fixed, paraffin-embedd
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3120-2017·2017-09-20
Leica Biosystems Recalls Podoplanin Antibody Due to Temperature Excursion
Leica Biosystems Richmond Inc. is recalling four units of Podoplanin (D2-40 Mab) antibody because a delay in transit may have caused the product to be stored outside of required temperature limits.
Product
Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use. The Podoplanin (D2-40) antibody is intended for qualified laboratories to qualitatively identify by light microscopy the presence of associated antigens in s
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-3126-2017·2017-09-20
Leica Biosystems Recalls SOX-10 Antibody Due to Temperature Excursion
Leica Biosystems Richmond Inc. is recalling 37 units of SOX-10 (Polyclonal) antibody because a delay in transit may have caused the product to be stored outside of defined temperature requirements.
Product
Cell Marque, SOX-10 (Polyclonal), 7 mL, REF PA0813, IVD, This antibody is intended for in vitro diagnostic (IVD) use. SOX-10 Rabbit Polyclonal Primary Antibody is intended for laboratory use in the detection of the SOX-10 protein in formalin-fixed, paraffin-embedded tissue staine
Category
Medical Device
Distribution
Distributed nationwide