Food & Beverages
HIGH
FDA FOOD
Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens
No ingredient label. Product contains undeclared allergens (peanuts, almonds, cashew, and soy)
Taproom Gourmet
No ingredient
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
3,598 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 3,598
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Food & Beverages
HIGH
FDA FOOD
Taproom Gourmet Bulk Empire Mix Recall for undeclared tree-nut Allergens
No ingredient label. Product contains undeclared allergens (cashews, almonds, walnuts, Brazil nuts, pecans, pistachios)
Taproom Gourmet
No ingredient
Food & Beverages
HIGH
FDA FOOD
Kirkland Signature Ahi Tuna Wasabi Poke Recalled Over Listeria Risk
Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.
Kirkland Signature
Listeria monocytogenes.
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for 0 Units in 2025
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Perifix FX Epidural Tray Recall for Lid Misalignment in Catheter Connector
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Food & Beverages
HIGH
FDA FOOD
Taproom Gourmet 20lb Park Mix Recalled for No Ingredient Label, Allergens Unreported (2025)
Taproom Gourmet bulk Park Mix, distributed to NY, NJ, CT, CA, IL and FL, is recalled for undeclared allergens and no ingredient label. Consumers should not consume the product. Egress Capital Partners Inc. is handling refunds or replacements via email.
Taproom Gourmet
No ingredient
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recall Expands for Epidural Tray and Catheter Over Lid Positioning Issue (2025)
Potential for the lid of the catheter connector to be in the incorrect position.
B BRAUN MEDICAL
Potential for
Health & Personal Care
HIGH
FDA DEVICE
B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z
Potential for the lid of the catheter connector to be in the incorrect position.
B Braun Medical
Potential for
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems LOGIQ P10 Ultrasound Systems Recalled for 65 Units in 2025 Over UGAP Data Errors
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.
GE Medical Systems
The Ultrasound-Guided
Health & Personal Care
HIGH
FDA DEVICE
Cardinal Health 200 Salem Sump Gastroduodenal Tubes Recalled Worldwide for ARV Breakage
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.
Cardinal Health 200
Firm has
Health & Personal Care
HIGH
FDA DRUG
Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025
CGMP Deviations: Market complaints received for gritty texture (grainy)
Glenmark Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)
InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.
Enterix
InSure ONE
Food & Beverages
HIGH
FDA FOOD
D & M Smoked Fish Recalls 2,022 Haifa Cold Smoked Salmon 8 oz for Listeria Contamination (2025)
D & M Smoked Fish
Contaminated with
Food & Beverages
HIGH
FDA FOOD
Haifa Cold Smoked Sea Bass 8 oz Recalled for Listeria Contamination (2025)
Haifa
Contaminated with
Food & Beverages
HIGH
FDA FOOD
Lipton Green Tea Citrus Recalled for Undeclared Sugar in 2,854 Cases (2025)
Undeclared sugar in finished product-primary package does not reflect the product inside bottle.
Lipton
Undeclared sugar
Health & Personal Care
HIGH
FDA DEVICE
Percussionaire IPV In-Line Valve Recall Aims to Stop Use Over Leakage Risk in Ventilators
Percussionaire
IFU update;
Health & Personal Care
HIGH
FDA DEVICE
Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.
Baxter Healthcare
Affected oral/axillary
Health & Personal Care
HIGH
FDA DEVICE
CPM Medical Consultants Recalls 3,317 Fuse ULTRA Foot Plating System IFU Updates (2025)
CPM Medical Consultants
Instructions for
Health & Personal Care
HIGH
FDA DRUG
Park Avenue Compounding Phenylephrine HCI Syringes Recalled Over CGMP Violations
Park Avenue Compounding
CGMP Deviations