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. 2,660 recalls have been distributed to Massachusetts in the last 12 months.
Showing 14401–14420 of 29,284 recalls
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/o Ind Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...
The Issue: Potential for products to fail performance testing per the Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...
The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...
The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...
The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD WAVELINQ 4F EndoAVF System Recalled by Bard Peripheral Vascular Inc Due...
The Issue: The firm has become aware of a potential problem with their venous and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posey Connected Twice-As-Tough Cuffs Recalled by TIDI PRODUCTS Due to Not...
The Issue: Not meeting design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...
The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...
The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Geistlich Bio-Oss Pen Recalled by Geistlich Pharma North America, Inc. Due...
The Issue: When unscrewing the green cap from the pen, a visible piece of green plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks...
The Issue: Gas springs not always replaced within the interval specified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIBotics iBlock Cutting Guide Recalled by OMNIlife science Inc. Due to The...
The Issue: The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical Inc Due to Failure...
The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical Inc Due to...
The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Certain lots were mislabeled with incorrect product number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.