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. 1,103 recalls have been distributed to Massachusetts in the last 12 months.
Showing 14361–14380 of 52,647 recalls
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...
The Issue: In instances where custom ranges were configured on the device post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QMS Tacrolimus Immunoassay CALIBRATOR SET QMS TACROLIMUS CAL Recalled by...
The Issue: Due to QMS Tacrolimus Calibrator recovering between 82 to 94% of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...
The Issue: Potential for Fluid Leak inside a staining system that could cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...
The Issue: Due to a component in the hemodialysis console there is the possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: YelloPort Elite 12x75 Pencil Point Trocar/ET1207503 Recalled...
The Issue: Laparoscopic devices have a sterile symbol included on labels but devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Siemens Medical Solutions USA, Inc....
The Issue: The clip store function in the ultrasound imaging system does not work when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SyncVision Systems Recalled by Volcano Corporation Due to If FFR...
The Issue: If FFR measurement(s) are made prior to an iFR/FFR co-registration/pullback...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bortezomib Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed stability specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amy's Vegan Organic Rice Mac & Cheese Recalled by Amys Kitchen Inc Due to...
The Issue: Firm investigation detected trace amounts of milk through finished product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10...
The Issue: Failed Dissolution Specification: Dissolution results are below...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINQ II Insertable Cardiac Monitor Recalled by Medtronic Inc., Cardiac...
The Issue: Devices may lose functionality due to susceptibility to moisture ingress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions...
The Issue: individual components have been labelled with incorrect colours. The red and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPAQUE Herrick Lacrimal Plugs Recalled by Lacrimedics Inc Due to The sterile...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Collagen Plugs Recalled by Lacrimedics Inc Due to The sterile pouch seal may...
The Issue: The sterile pouch seal may contain channels that could affect the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox delta Ceramic V40 Femoral Head 32/ -4.0mm Catalog Number: 6570-0-032...
The Issue: Potential product mix where the size and/or offset of the Biolox delta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1688 Camera Control Unit (CCU) Recalled by Stryker Corporation Due to A...
The Issue: A software defect in the camera control unit (CCU) will cause the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.