Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 28461–28480 of 52,535 recalls
Recalled Item: GE Healthcare Centricity PACS-IW Recalled by GE Healthcare Due to A database...
The Issue: A database handling error could occur during the image acquisition process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T4 Pullover Toga Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Separation of material layers may occur, causing a potential risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain...
The Issue: Wire sets of certain devices were assembled with adhesive on the contact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REPAIR KIT Recalled by Medical Components, Inc dba MedComp Due to There is...
The Issue: There is the potential for connection failures related to the female...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life Change Fat Burner Recalled by Get The Tea Due to Get The Tea is...
The Issue: Get The Tea is notifying customers that Life Change Fat Burners contain soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thyroid Resilience 120 count bottle packaged in an amber plastic Recalled by...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Testosterzone 180 count bottle packaged in an amber plastic bottle Recalled...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white...
The Issue: Recalled dietary supplements may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pink flexible Recalled by Ikea North America Srvcs Inc Due to Possible Pest...
The Issue: Possible Pest Contamination at production facility.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and Recalled...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221<4>Roche OMNI S4 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221<6>Roche OMNI S6 system Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas b 221 AutoQC Module Complete Recalled by Roche Diagnostics Corporation...
The Issue: The software responsible for starting scheduled AutoQC measurements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 125II Assay Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Upon dilution, some patient samples may exhibit over-recovery outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution Recalled by Draegar...
The Issue: The invasive pressure visual and audible alarms may not activate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra-Aortic Balloon Catheter Mega 8FR 50cc Product Usage: The intra-aortic...
The Issue: The U.S. Instructions For Use for the Mega Intra-Aortic Balloon (IAB)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: clariti 1 day (-1.25) 90 pack Recalled by CooperVision Inc. Due to The...
The Issue: The secondary packaging is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.