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. 2,631 recalls have been distributed to Massachusetts in the last 12 months.
Showing 16601–16620 of 29,284 recalls
Recalled Item: OviTex 2S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 20x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 18x22cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 4x8cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 6x10cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 10x20cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 10x12cm Recalled by AROA Biosurgery, LTD....
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 16x20cm Recalled by AROA Biosurgery, LTD. Due...
The Issue: Degradation of the PGA suture material used in the manufacture of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Recalled...
The Issue: The retail shelf cartons may be labeled with an incorrect lot number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...
The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...
The Issue: The DC power to the IFOSS collision detector control panel at your facility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...
The Issue: Unusually high number of total images/unassigned events may require...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...
The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.