Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,736 recalls have been distributed to Massachusetts in the last 12 months.
Showing 3661–3680 of 52,647 recalls
Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...
The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...
The Issue: Complaints have been received regarding post-operative implant collapse.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clobazam Tablets Recalled by Amerisource Health Services LLC Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion GBS Assay Kit containing Panther Fusion Recalled by Hologic,...
The Issue: Potential weak pouch seal on Panther Fusion GBS assay cartridge, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THREE RIVERS brand TUTTI-FRUTTI Recalled by Shata Traders Inc. Due to...
The Issue: Product contains undeclared FD&C Yellow 5 and FD&C Yellow 6.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acetaminophen Recalled by Akron Pharma, Inc. Due to Labeling: Not Elsewhere...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 50 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Regular Strength Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diphenhydramine HCl 25 mg Recalled by Akron Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Extra Strength 500 mg Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.