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. 2,012 recalls have been distributed to Massachusetts in the last 12 months.
Showing 5901–5920 of 29,284 recalls
Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...
The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...
The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...
The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Aneurysm Clip TITANIUM Paddle-Clip Recalled by Peter Lazic Gmbh Due to...
The Issue: Wrong product coloring. The paddle clips should be blank, but they are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace2- Indicated for use as an adjunct to seizure monitoring Recalled by...
The Issue: May have a battery life lasting less than the full 48 hours, requiring the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP Family 50 Series Models as follows: In vitro Recalled by...
The Issue: Sample misidentification could occur under specific conditions and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Redwood 2.0 ultrasound systems Recalled by Siemens Medical Solutions...
The Issue: If a user-generated preset for an 18L6 transducer created on a 1.0...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Libre 2 Readers Recalled by Abbott Diabetes Care, Inc. Due to If...
The Issue: If blood glucose monitoring system users attempt to start a new sensor, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD HORIZON Spinal System Solera Awl Tip Tap Recalled by Medtronic Sofamor...
The Issue: Incorrect Laser Marking - Solera Awl Tip Tap
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to Lipemic interference...
The Issue: Lipemic interference failed to meet the performance specification listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX ALIF S/A Recalled by Medicrea International Due to There is a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PASS LP Recalled by Medicrea International Due to There is a potential for a...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX TLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX 3D Recalled by Medicrea International Due to There is a potential for...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPIX DLIF Recalled by Medicrea International Due to There is a potential...
The Issue: There is a potential for a product packaging non-conformity issue which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.