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. 2,715 recalls have been distributed to Massachusetts in the last 12 months.
Showing 6561–6580 of 29,284 recalls
Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...
The Issue: The error resulted in intermittent failure of current (primary) radiology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Respiratory Panel 2.1 (RP2.1) Recalled by BioFire Diagnostics, LLC...
The Issue: Due to manufacturing issue, panels may result in false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Due to manufacturing issue, panels may result in false negative results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....
The Issue: Potential to cause biased results in the upper end of the reportable range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Kit Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Defibrillator/pacemaker module (DPM) may encounter a problem causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...
The Issue: Vyaire Medical identified two patient safety risks during the use of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...
The Issue: Drill guides might bend when axial forces are applied by surgeon during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended Recalled...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230 CM 10/BX- Intended Recalled...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for...
The Issue: Complaints on clip deployment occurring during clinical procedures, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.