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. 2,710 recalls have been distributed to Massachusetts in the last 12 months.
Showing 8781–8800 of 52,647 recalls
Recalled Item: Tizanidine Tablets Recalled by Amerisource Health Services LLC Due to Failed...
The Issue: Failed Dissolution Specifications: this repackaged product was recalled by...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1/2 gallon CN Smith brand Apple Cider Recalled by Bevovations, LLC Due to...
The Issue: Product contains high levels of patulin (above 50ppb).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UroLift Visual Obturator Recalled by Scholly Fiberoptic Gmbh Due to There is...
The Issue: There is an improperly performed weld between the cone of the sheath lock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellacor System with Micro-Coring Technology-Indicated for use by medical...
The Issue: Potential failure of a bearing adhesive joint that can occur due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes: (1) Ecolab Banded Bag with Rubberband and Tape...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equipment and table drapes and Surgical Room Turnover (SRT) Kits: Recalled...
The Issue: Certain lots of the products have a Naphthalene odor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINEAR 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION 7 Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YAMATO PLUS IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 7.5Fr IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANS-RAY IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 7.5Fr.IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REINFORCED INTRODUCER SET Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGA 8Fr. IAB Recalled by Datascope Corp. Due to During IAB catheter...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSATION PLUS 8Fr. IAB Recalled by Datascope Corp. Due to During IAB...
The Issue: During IAB catheter insertion, the introducer dilator may fracture at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by ALEMBIC PHARMACEUTICALS,...
The Issue: Defective Delivery System
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: INFX-8000C XGCP-930AA TABLE SIDE CONSOLE Recalled by Canon Medical System,...
The Issue: The C-arm, used to set the position and angle of the x-ray exposure field,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Tips Set Device Recalled by Creganna Medical Devices Due to Three lots...
The Issue: Three lots of product may be labeled with an incorrect expiration day
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STATCLAVE G4 Chamber Autoclave -Tabletop steam sterilizer intended for use...
The Issue: The STATCLAVE G4 is a dynamic air removal (prevacuum) tabletop steam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.