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. 2,527 recalls have been distributed to Massachusetts in the last 12 months.
Showing 33301–33320 of 52,647 recalls
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...
The Issue: Accuray has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnLite Neonatal TREC Kit Recalled by PerkinElmer Health Sciences, Inc. Due...
The Issue: Unique Device Identifier (UDI) is missing from outer kit box label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...
The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sweet Cream Buttermilk Powder in 50 # bags Recalled by Valley Milk Products...
The Issue: Products are recalled due to potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Non Fat Dry Milk Recalled by Valley Milk Products Due to Potential...
The Issue: Products are recalled due to potential Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...
The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...
The Issue: A quality issue with the junction box used in the bariatric bed junction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...
The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...
The Issue: Edits to Particle field definition parameters may not be saved when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.