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. 2,727 recalls have been distributed to Maryland in the last 12 months.
Showing 19761–19780 of 29,093 recalls
Recalled Item: 6.8cm Controlled Depth Attachment Product Usage: Pneumatic system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Handpiece EM Hand Control Product Usage: Electric system Recalled...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keyless Driver Product Usage: Pneumatic system Recalled by The Anspach...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reciprocating MICRO SAW Recalled by The Anspach Effort, Inc. Due to Supplied...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foot Control without Switches Recalled by The Anspach Effort, Inc. Due to...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Adult Craniotome Product Usage: Pneumatic system Recalled by The...
The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCC Soft Computer Softbank II software Product Usage: Supports single...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Softbank software Product Usage: Decision support software for transfusion...
The Issue: Software error. Potential for incorrect results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F STRAIGHT S61CM D66CM Catalog # AB10218 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 8F C70¿ S61CM D66CM Catalog # AB081041 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...
The Issue: The device defect is a positive bias of up to 20% relative to the currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S79CM D84CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C90¿ S61CM D66CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C90¿ S79CM D84CM Catalog # AB101078 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.