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. 2,511 recalls have been distributed to Massachusetts in the last 12 months.
Showing 35961–35980 of 52,647 recalls
Recalled Item: EXPANDED 5/18/2016 DAKOTA STYLE Salted Caramel sunflower kernel 2000 lbs....
The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2nd EXPANSION 5/31/2016 Product shipped OUS only. Light Salt Sunflower...
The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DAKOTA STYLE SAVORY BACON sunflower kernel 2000 lbs. Poly Lined Recalled by...
The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2nd EXPANSION 5/31/2016 Navitas Naturals Recalled by SunOpta Food and Grain,...
The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 2nd EXPANSION 5/31/2016 Product shipped OUS only. Spitz Dill Pickle Recalled...
The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...
The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...
The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...
The Issue: Labeling errors. The outer packge label expiration date may exceed the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...
The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...
The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.