Health & Personal Care
HIGH
FDA DEVICE
Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
Boston Scientific
Certain desiccant
Recall database
All Product Recalls
Browse 4,420 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
- Active recalls
- 4,420
- Current page
- 202
Health & Personal Care
HIGH
FDA DRUG
Chlorpromazine Hydrochloride 200 mg Recall Expanded After Packaging Contamination Found in 3,363 JDS
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal 800mg/160mg Sulfamethoxazole and Trimethoprim Tablets Recalled for Foreign Packaging Material
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride 25 mg 100-count Recalled in 2025 for Packaging Contamination
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride Recall 2025: 14,923 Bottles Over Packaging Contamination
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific ICEfx Cryoablation System Recalled for 19 Units Worldwide (2025)
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
Boston Scientific
Certain desiccant
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride 50 mg Tablets Recall 2025 (13,130 Bottles)
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
B. Braun Lactated Ringers Injection 46,032 Containers Recalled Over Particulate Matter
B Braun Medical
Presence of
Health & Personal Care
HIGH
FDA DRUG
B. Braun Sodium Chloride Injection 1000 mL Recalled nationwide for particulates (Class I)
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
B. Braun Medical Inc.
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Aesculap ELAN 4 Fixed Duraguard Recalled for Mislabeling (1 Unit, 2025)
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Aesculap AG
Mislabeling. The
Health & Personal Care
HIGH
FDA DEVICE
Corneat Vision EverPatch+ 180-Unit Recall for Scleral Patch Dehiscence Risk (2025)
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
CORNEAT VISION
Reviewed complaints
Health & Personal Care
HIGH
FDA DEVICE
CorNeat Vision EverPatch Recalled for Conjunctival Wound Dehiscence Risk (630 Units, 2025)
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
CorNeat Vision
Reviewed complaints
Health & Personal Care
HIGH
FDA DEVICE
Aesculap AG Recalls ELAN 4 Fixed Duraguard Long Mislabeling Devices (GB943R)
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Aesculap AG
Mislabeling. The
Food & Beverages
HIGH
FDA FOOD
Tampa Maid Foods Frozen Shrimp Recalled for Cs-137 Contamination (2025)
Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp due to potential Cesium-137 contamination. The product was distributed to 16 states. Consumers should not eat the shrimp and should contact the company for refunds or replacements.
TAMPA MAID FOODS
Product may
Food & Beverages
HIGH
FDA FOOD
Tampa Maid Foods Recalls 31 Cases of Clean-tail Coconut Farm Breaded Butterfly Shrimp for Cs-137Cont
Product may be contaminated with Cesium-137 (Cs-137)
Tampa Maid Foods
Product may
Food & Beverages
HIGH
FDA FOOD
ADMIRAL OF THE FLEET, PORTICO SEAFOOD CLASSIC Breaded Shrimp Recalled Over Cs-137 Contamination (120
Product may be contaminated with Cesium-137 (Cs-137)
ADMIRAL OF THE FLEET
Product may
Health & Personal Care
HIGH
FDA DEVICE
Mindray BeneVision N1 Patient Monitor Recall Issued for 2,278 Units Worldwide (2025)
Potential for activation of an abnormal alarm pause.
Mindray
Potential for
Health & Personal Care
HIGH
FDA DEVICE
Maquet Cardiovascular Recalls 16,512 Heartstring III Seal Systems Over Hemostasis Failure
Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.
Maquet Cardiovascular
Three failure
Health & Personal Care
HIGH
FDA DEVICE
Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)
Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.
Maquet Cardiovascular
Three failure
Food & Beverages
HIGH
FDA FOOD
Anderson Candy Company Recalls 960,000 Peanut Rounds for Undeclared Soy Allergen (2025)
Anderson Candy Company
Undeclared soy