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. 2,678 recalls have been distributed to Massachusetts in the last 12 months.
Showing 12101–12120 of 29,284 recalls
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...
The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic Recalled...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental...
The Issue: Restorations crack during the sintering process.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...
The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...
The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.