stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

Fisher & Paykel Recall 51,144 Airvo 2 and myAirvo 2 Humidifiers Over Power-Disconnect Audible Alert

Fisher & Paykel Healthcare recalled 51,144 Airvo 2 and myAirvo 2 humidifiers in the United States. The devices may emit an audible alert for less than 120 seconds after power is disconnected. This could delay user awareness to reconnect power and lead to oxygen desaturation. Patients and healthcare providers should stop using the device and await manufacturer instructions.

Fisher & Paykel Healthcare
When unintentionally
Read more
Health & Personal Care
HIGH
FDA DRUG

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

Glenmark Pharmaceuticals Inc. USA recalls 13,824 tubes of azelaic acid gel 15% after CGMP deviations prompted gritty texture complaints. The recall covers nationwide distribution in the United States. Consumers should stop using the product and contact Glenmark for guidance.

Glenmark Pharmaceuticals
CGMP Deviations:
Read more
Health & Personal Care
HIGH
FDA DRUG

Park Avenue Compounding Phenylephrine HCI Syringes Recalled Over CGMP Violations

Park Avenue Compounding recalled 858 syringes of Phenylephrine HCI on September 17, 2025, due to CGMP deviations. The recall affects syringes with Lot # 20250813-13D65E and an expiration date of February 9, 2026. Consumers must stop using the product immediately and consult healthcare providers for further guidance.

Park Avenue Compounding
CGMP Deviations
Read more
Food & Beverages
HIGH
FDA FOOD

Haifa Cold Smoked Sea Bass 8 oz Recalled for Listeria Contamination (2025)

Haifa Cold Smoked Sea Bass 8 oz distributed by D & M Smoked Fish is recalled after 348 pieces were found contaminated with Listeria monocytogenes. The recall was issued Sept. 17, 2025, with FDA update on Oct. 22, 2025. Consumers should not eat the product and should contact D & M Smoked Fish for refunds or replacements.

Haifa
Contaminated with
Read more
Food & Beverages
HIGH
FDA FOOD

Lipton Green Tea Citrus Recalled for Undeclared Sugar in 2,854 Cases (2025)

PepsiCo's Lipton Green Tea Citrus RTD bottles, sold at multiple retailers, are recalled after undeclared sugar was found in the finished product. A labeling error shows 25g sugar on the outer case while individual bottle labels show 0g. Consumers should not drink this product and should contact PepsiCo for refunds or replacements.

Lipton
Undeclared sugar
Read more
Health & Personal Care
HIGH
FDA DEVICE

Enterix InSure ONE FIT Recall Affects 201,426 Tests Over False Negatives (2025)

Enterix recalled 201,426 InSure ONE Fecal Immunochemical Test kits after a sensitivity failure linked to Test Card Lot TT241102. The issue may cause false negative results. Healthcare providers and patients should stop using the affected kits and follow the manufacturer’s recall instructions.

Enterix
InSure ONE
Read more
Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Baxter Healthcare recalled 5,209 oral/axillary probes used with Welch Allyn SureTemp Plus thermometers nationwide in the United States, Canada and Colombia. The probes were inadvertently programmed with the rectal configuration, which can yield a lower temperature reading. Healthcare providers and patients should stop using the affected probes immediately and follow Baxter’s recall instructions.

Baxter Healthcare
Affected oral/axillary
Read more
Food & Beverages
HIGH
FDA FOOD

Sprout Organics 6+ Months Baby Food Recalled for Lead Contamination in 9,873 Cases (2025)

Sprout Organics recalled 9,873 cases of 6+ Months Made With Organic Sweet Potato, Apple & Spinach baby food nationwide. A potential contamination with lead has been identified. Consumers who purchased the product should stop using it and contact Sprout Organics for refund or replacement through the recall notice.

Sprout Organics
Potential contamination
Read more
Health & Personal Care
HIGH
FDA DRUG

Accord Healthcare Recalls 54,432 Levothyroxine 88 mcg Tablets for Subpotent Potency (2025)

Accord Healthcare recalled 54,432 bottles of Levothyroxine Sodium Tablets, USP, 88 mcg, distributed nationwide in the United States. The recall is due to subpotent assay content observed during long-term stability testing. Patients should stop using the product immediately and contact Accord Healthcare or their healthcare provider for guidance.

Levothyroxine Sodium
Subpotent: During
Read more
Food & Beverages
HIGH
FDA FOOD

Lawrence Wholesale Frozen Shrimp Recalled for Cs-137 Contamination (4,871 Cases, 2025)

Lawrence Wholesale recalled 4,871 cases of frozen tail-on shrimp sold through Kroger stores in 16 states. The products were manufactured under insanitary conditions and may be contaminated with Cesium-137. Consumers should not eat these shrimp and should contact Lawrence Wholesale LLC for refunds or replacements.

Lawrence Wholesale
Product manufactured
Read more
Food & Beverages
HIGH
FDA FOOD

Lawrence Wholesale Shrimp Cocktail Bowls Recalled for Cs-137 Contamination Risk (2025)

Lawrence Wholesale recalled 8,400 cases of Shrimp Cocktail Bowl products sold to Kroger stores in 15 states on Sept. 16, 2025 due to potential Cesium-137 contamination. The recall involves 7oz and 17oz clear plastic bowls with UPCs 011110622952 and 011110624840. Consumers should not consume the product and should contact Lawrence Wholesale LLC for refund or replacement by email.

Lawrence Wholesale
Product manufactured
Read more
Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella Automated Controller Recall Affects 9,177 Units Worldwide (2025)

Abiomed recalled 9,177 distributed Automated Impella Controllers worldwide over purge pressure concerns linked to purge retainer failures. The recall covers multiple product codes, including AIC w/Impella Connect for ECP (1000432) and various packaged controllers. Hospitals and clinicians should stop using the device and follow the manufacturer's recall instructions immediately.

Abiomed
Potential for
Read more
Health & Personal Care
HIGH
FDA DRUG

IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide

IntegraDose Compounding Services recalled 853 IV bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride. The recall is nationwide in the United States. Testing found no oxytocin in the IV bags. Stop using the product and contact IntegraDose or a healthcare provider for guidance.

IntegraDose Compounding Services
Subpotent Drug:
Read more
Health & Personal Care
HIGH
FDA DRUG

Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)

Graviti Pharmaceuticals Private Limited manufactured Bupropion Hydrochloride Extended-Release Tablets XL 300 mg, distributed nationwide by Rising Pharma Holdings, Inc., in 46,512 bottles. The recall cites failed tablet specifications. Stop using the product immediately and contact the manufacturer or your healthcare provider for guidance.

Bupropion Hydrochloride
Failed Tablet/Capsule
Read more
Health & Personal Care
HIGH
FDA DEVICE

Alcon CONSTELLATION Ultravit 10K & HyperVit 20K Recall for 28,323 Units (2025)

Alcon recalls 28,323 CONSTELLATION Ultravit 10K and CONSTELLATION HyperVit 20K devices used in hospitals worldwide. The recall lists an unspecified hazard. Hospitals should stop using the devices immediately and follow the manufacturer’s instructions. Access the FDA recall notice for details.

Alcon
XXX
Read more
Health & Personal Care
HIGH
FDA DRUG

Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser after detecting elevated benzene levels. The recall covers products associated with Lot # 58170A and Lot # 58172A distributed in CA and GA. Consumers should stop use and seek guidance from a healthcare provider.

Skin MD
Chemical Contamination:
Read more
Previous
12345...108
Next

Tag Statistics

Total Recalls
2,153

Related Tags

electronicbattery poweredimmediate actionreturn for refundreplacement availableinfant productadult productbedroomworkplacechemical hazardpoisoning riskcpsc regulated