Hazard

Contamination recalls

2,060 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 2,060
Critical: 83
Severe: 615
Most recent: 2026-09-09

Of the 2,060 contamination recalls we have scored against our rubric, 83 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 615 (30%) 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 contamination 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.

551–575 of 2060

HighFDA (Devices)·Z-0931-2022·2022-04-20
Siemens Atellica CH Lithium reagent recalled for potential reagent carryover
Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.
Product
Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0926-2022·2022-04-20
Philips Autoclavable Temperature Probes: Updated Cleaning Instructions
Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.
Product
The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0862-2022·2022-04-13
Neurological surgical kits may have compromised packaging sterility
Stradis Medical is recalling Surgicare Neuro Pack neurological kits because the outer bag may be perforated or torn, potentially compromising product sterility. 176 units were distributed in Indiana, Texas, and Pennsylvania.
Product
Surgicare Neuro Pack - Neurological Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0866-2022·2022-04-13
Surgical kit recall due to outer bag perforation and sterility risk
Stradis Medical is recalling 348 units of its Total Joint Pack Surgical Kit due to risk of outer bag tears or perforations that could compromise kit sterility. The recall affects units distributed in Indiana, Texas, and Pennsylvania.
Product
Coryell Memorial Hosp Total, Joint Pack - Surgical Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0733-2022·2022-04-06
Injectable Testosterone Recalled Due to Lack of Sterility Assurance
Drug Depot's testosterone injection product was recalled nationwide for lack of sterility assurance. Affected consumers should discontinue use and consult their healthcare provider.
Product
TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable, Packaged in a multi dose 10ml vial, Formula ID 115498, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0665-2022·2022-03-23
Lorazepam 1 mg/mL Infusion Solution Recalled for Lack of Sterility Assurance
Family Pharmacy of Statesville is recalling Lorazepam 1 mg/mL Infusion Solution in 250 mL bags because the manufacturer cannot assure sterility of the product.
Product
Lorazepam 1 mg/mL Infusion Solution in 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0656-2022·2022-03-23
Hydromorphone HCl Infusion Bags Recalled for Lack of Sterility Assurance
Family Pharmacy of Statesville is recalling Hydromorphone HCl 2 mg/mL Infusion 250 mL bags (2 units) distributed in North Carolina due to lack of assurance of sterility.
Product
Hydromorphone HCl 2 mg/mL Infusion 250 mL bags, Rx only, Family Pharmacy of Statesville, Inc.
Category
Drug
Distribution
1 state
HighFDA (Devices)·Z-0766-2022·2022-03-23
Boston Scientific recalls 68 medical devices with sterility breach
Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.
Product
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2022·2022-03-23
HYDRATOME RX surgical device recalled due to sterile barrier breach
Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.
Product
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0779-2022·2022-03-23
Boston Scientific JAGTOME RX Device Recalled for Sterile Barrier Breach
Boston Scientific is recalling 14 JAGTOME RX medical devices worldwide due to a sterile barrier breach that compromises the device's sterility.
Product
JAGTOME RX 49-30-450-035 Material Number: M00573030
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2022·2022-03-16
FDA Recalls Diagnostic Test Strips for False Positive Results
NeuMoDx COVID-19 test strips (Lot 116305 S/L-02) are recalled due to product contamination that increases risk of false positive results. The recall affects 102 boxes distributed in FL, MD, MI, and NY.
Product
NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip, Ref # 300900 (marketed under EUA202947). Distributed in boxes of 6 assay strips in individual pouches. Box, pouch and strips all labeled with product name, ref #, lot #, and expiration date.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0703-2022·2022-03-09
QC Control Sets for GBS Testing Recalled Due to Contamination
Microbiologics QC sets used for GBS testing contain a negative control contaminated with Group B Streptococcus, causing test failures. Affects 541 units distributed nationwide.
Product
QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set (Live Culture). Sets include: 1. 0864E3 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 2. 0864E5 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 3. 0864E7 Streptococcus agalactiae (Gro
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0780-2022·2022-03-02
Kroger veggie blend recalled for Listeria contamination from harvest equipment
Dole Fresh Vegetables Inc is recalling Kroger 12 oz Veggie Blend after harvest equipment tested positive for Listeria monocytogenes. The affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.
Product
Kroger 12 oz Veggie Blend UPC: 0-11110-91048-6 SKU: 3013
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-0669-2022·2022-03-02
RESODURA Matrix Onlay Recalled Due to Unsealed Packaging
Collagen Matrix is recalling RESODURA matrix onlay dural substitutes due to outer packaging that is not properly sealed, potentially compromising sterility and creating a risk of infection.
Product
RESODURA matrix onlay 10.0 cm x 12.5 cm - indicated as dural substitutes for the repair of dura matter. REF: DUMO10125
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0628-2022·2022-03-02
Nasal Spray Oxymetazoline HCl Recalled Due to Contaminated Excipient
Perrigo Company PLC is recalling Nasal Maximum Strength Nasal Spray (Oxymetazoline HCl 0.05%) due to contamination from a recalled excipient used during manufacturing. Approximately 2,302 bottles were distributed nationwide.
Product
NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0596-2022·2022-03-02
Infants Pain and Fever acetaminophen recalled for contaminated excipient
Perrigo Company is recalling Infants Pain and Fever acetaminophen oral suspension (160mg/5ml) distributed nationwide due to contamination from a recalled excipient supplier. The product was manufactured with a contaminated ingredient that does not meet manufacturing standards.
Product
INFANTS PAIN AND FEVER — INFANTS PAIN AND FEVER (ACETAMINOPHEN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0578-2022·2022-02-23
Chlorthalidone Tablets Recalled for Foreign Matter Contamination
Sun Pharmaceutical is recalling Chlorthalidone Tablets USP 25 mg (Lot #P0602, expiration 03/2023) due to stainless steel microscopic wear particles, punch lubricant oil, and silicone particles from the dust cup found in the product.
Product
CHLORTHALIDONE — CHLORTHALIDONE (CHLORTHALIDONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0561-2022·2022-02-16
Gentueri Viral Transport Medium Kit recalled due to sterility failure
Gentueri Inc is recalling Viral Transport Medium Kits due to failed sterility testing and evidence of contamination. The recall affects 13,975 units distributed to Illinois, Nebraska, and Wisconsin.
Product
Gentueri Viral Transport Medium Kit with 8cm Breakpoint Swab
Category
Medical Device
Distribution
3 states
SevereFDA (Drugs)·D-0424-2022·2022-02-02
Vancomycin HCl Ophthalmic Solution Recalled for Sterility Assurance
Edge Pharma LLC is recalling Vancomycin HCl sterile ophthalmic solution for injection due to lack of assurance of sterility. The affected product was distributed nationwide.
Product
Vancomycin HCl, Sterile Ophthalmic Solution for Injection, Preservative Free, 8 mg/0.8mL (10 mg/mL) (vancomycin equivalent), 0.8 mL per syringe, Single Use Syringe, For Intraocular Injection, Edge Pharma LLC, 856 Hercules Dr., Colchester, VT, 05446, NDC 05446-0736-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0556-2022·2022-02-02
Crisp Greens Salad Recalled for Potential Listeria Monocytogenes Contamination
Fresh Express Inc is recalling Crisp Greens salad in 12oz. packages due to potential contamination with Listeria monocytogenes. The recall affects products distributed to domestic and Canadian distributors across 20 U.S. states.
Product
"Crisp Greens" (salad product) packed in 12oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0600-2022·2022-02-02
Fresh Express Spring Mix Salad Recalled for Listeria Risk
Fresh Express Inc is recalling Spring Mix salad in multiple package sizes due to potential Listeria monocytogenes contamination. The product was distributed across the United States and Canada.
Product
"Spring Mix" (salad product) packed in 5oz., 10oz., 11oz., and 16oz. packages
Category
Food
Distribution
20 states
SevereFDA (Food)·F-0584-2022·2022-02-02
Organic Spring Mix Salad Recalled Due to Listeria Contamination Risk
Fresh Express Inc is recalling Organic Spring Mix salad in 5oz., 10oz., and 16oz. packages due to potential Listeria monocytogenes contamination. Affected products were distributed to retailers and distributors across 20 US states and Canada.
Product
"Organic Spring Mix" (salad product) packed in 5oz., 10oz., and 16oz. packages
Category
Food
Distribution
20 states
SevereFDA (Drugs)·D-0407-2022·2022-02-02
Mitomycin-C Injectable Syringes Recalled for Sterility Assurance Failure
Edge Pharma is recalling Mitomycin-C 40 mg/40 mL single-dose syringes (NDC 05446-1416-01) nationwide due to lack of assurance of sterility. Approximately 860 syringes are affected.
Product
Mitomycin-C, 40mg/40mL (1mg/mL), 40 mL per syringe, Single Dose Syringe for Intravesical Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1416-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0576-2022·2022-02-02
Fresh Express Organic Baby Spinach & Kale Mix Recall: Listeria Risk
Fresh Express Inc is recalling "Organic Baby Spinach & Baby Kale Mix" salad in 5oz packages due to potential contamination with Listeria monocytogenes. The affected product was distributed to over 110 domestic distributors across multiple states and Canada.
Product
"Organic Baby Spinach & Baby Kale Mix" (salad product) packed in 5oz. packages
Category
Food
Distribution
20 states
SevereFDA (Drugs)·D-0411-2022·2022-02-02
Neostigmine Methylsulfate Injectable Syringes Recalled for Sterility Assurance
Edge Pharma, LLC is recalling Neostigmine methylsulfate 5 mg/5mL single-use syringes for IV or IM injection due to lack of assurance of sterility. Approximately 160 syringes nationwide may be affected.
Product
Neostigmine methylsulfate, 5 mg/5mL (1 mg/mL), 5 mL per syringe, Single Use Syringe for IV or IM Injection, Edge Pharma, LLC, 856 Hercules Dr. Colchester, VT 05446, NDC 05446-1549-05
Category
Drug
Distribution
Distributed nationwide