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. 2,716 recalls have been distributed to Maryland in the last 12 months.
Showing 22281–22300 of 29,093 recalls
Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...
The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO Radiation Treatment Planning System. Used to create treatment plans...
The Issue: Incorrect Treatment Delivery Using Third Party Fixed Wedges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Free T3 Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Medical Systems Duodenoscope Recalled by Fujifilm Medical Systems...
The Issue: A precautionary measure because the Duodenoscopes have been redesigned to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of tests associated with the affected lots(...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.