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. 2,511 recalls have been distributed to Massachusetts in the last 12 months.
Showing 36521–36540 of 52,647 recalls
Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....
The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hardy Diagnostics GBS Detect Cat no. A300. Used for the Recalled by Hardy...
The Issue: Performance failure; poor hemolytic reaction of non or weakly hemolytic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...
The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...
The Issue: The affected scanner does not correctly interact with the SC360 software....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as an insect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gingko Biloba 60mg packaged in a white and orange bottle Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Goldenseal Root 500 mg packaged in a white and orange Recalled by NOW Foods...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elderberry 500 mg packaged in a white and orange bottle Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cranberry extract packaged in a white and orange bottle containing Recalled...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Andrographis extract 400 mg packaged in a white and orange Recalled by NOW...
The Issue: Undeclared soy lecithin in 5 dietary supplements.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...
The Issue: The device may have a defect in the catheter. In some instances this defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...
The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD-Retic-Count Reticulocyte Reagent System Recalled by Becton, Dickinson and...
The Issue: The carton label for one lot of BD Retic-Count Reticulocyte Reagent System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 134 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 200 mg Recalled by Impax Laboratories,...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Newport Creamery Coffee Ice Cream Recalled by Bliss Bros Dairy, Inc. Due to...
The Issue: Product failed to meet air space specifications
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cresent Ridge Vanilla Ice Cream 3gal Product Code: 36100 Recalled by Bliss...
The Issue: Product failed to meet air space specifications
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Emack & Bolios Serious Choc Addiction Ice Cream 3gal Product Code: 36271...
The Issue: Product failed to meet air space specifications
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cresent Ridge Oreo Cookie Ice Cream 48oz Product Code: 35424 Recalled by...
The Issue: Product failed to meet air space specifications
Recommended Action: Do not consume. Return to store for a refund or discard.