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. 2,547 recalls have been distributed to Massachusetts in the last 12 months.
Showing 22101–22120 of 29,284 recalls
Recalled Item: Reagent Management System (RMS) Dimension RxL Max HM STM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost stationary X-ray system Recalled by Philips...
The Issue: The detector may signal that it is ready for acquisition when it actually is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension EXL with LM Product Usage:...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...
The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...
The Issue: The product may contain electronic components that lead to a premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...
The Issue: Testing at customer site showed unit Remote Patient Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...
The Issue: Based on internal investigation and testing that revealed the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...
The Issue: Antibiotic concentration may be insufficient which may result in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...
The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys spine Recalled by Genesys Orthopedics Systems, LLC Due to...
The Issue: Unanticipated technique for a cervical screw insertion caused the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump SmartSite Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...
The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 DL380 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLINIC PATCH 3.3.0 CD Product Usage: MYLA is a Recalled by bioMerieux,...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA CLI V3.X TO V4.1 ML350 SERVER Product Usage: MYLA Recalled by...
The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.