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. 2,542 recalls have been distributed to Massachusetts in the last 12 months.
Showing 27121–27140 of 52,647 recalls
Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...
The Issue: The device accessories were not labeled with appropriate latex warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...
The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...
The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Recalled by...
The Issue: Expired intraocular lenses were distributed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...
The Issue: A portion of this lot was manufactured using Gentamicin instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.