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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.
Showing 28281–28300 of 29,284 recalls
Recalled Item: Software for Vitrea Recalled by Vital Images, Inc. Due to Vital Images has...
The Issue: Vital Images has found two potential errors in calcium score values in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progel Pleural Air Leak Sealant Recalled by Neomend Inc Due to Product was...
The Issue: Product was distributed with an incorrect expiration date. Product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...
The Issue: GE Healthcare became aware of a potential issue related to incorrect image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray A5 Anesthesia Delivery System Manufactured in China for Mindray...
The Issue: Mindray has identified the potential for a system leak resulting an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capsule Neuron Docking Station Recalled by Capsule Tech Inc. Due to Capsule...
The Issue: Capsule Neuron Docking Station may experience a lost connection, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS Urine BETA CrossLaps ELISA Recalled by Immunodiagnostics Systems Ltd Due...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QKC1692E The QKC1692E Quick Connect device connects endoscopes to the...
The Issue: STERIS has been actively seeking devices for quick connect revalidation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Control Set Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Ostase¿ BAP (Bone Alkaline Phosphatase) Recalled by...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Intact PINP Control Set Recalled by Immunodiagnostics Systems Ltd...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS Intact PINP Recalled by Immunodiagnostics Systems Ltd Due to It has...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDS-iSYS N-Mid¿ Osteocalcin Recalled by Immunodiagnostics Systems Ltd Due to...
The Issue: It has been noted by staff at IDS Inc. that stock of the affected products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyRay RXDC dental unit x-ray unit Recalled by CEFLA DENTAL GROUP Due to The...
The Issue: The RX DC dental x-ray unit was found to be noncompliant with 21CFR 1010,2,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...
The Issue: Loss of patient data can occur under certain circumstances due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra HRAIM Head Ring Assembly with Intubation Mounts The CRW Recalled by...
The Issue: T-handle screw is used on a complementary product to the CRW, the Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...
The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 TORQUE WRENCH Manufactured by: Stryker Recalled by Stryker...
The Issue: Multiple complaints have reported the hex tip of the torque wrench...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.