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. 2,774 recalls have been distributed to Maryland in the last 12 months.
Showing 18081–18100 of 29,093 recalls
Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nussloch GmbH ASP6025 Tissue Processor Recalled by Leica Microsystems, Inc....
The Issue: Incorrect labeling for specified voltage for the Alarm Connectors on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning...
The Issue: Incorrect PEC values.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...
The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100i Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp -...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...
The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 9"x100'. One roll per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 16"x16" Heat Seal Pouch 100 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 14"x100'. One roll per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 10.5"x28" Self Seal Pouch 100 pouches per box Recalled...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 8"x10" Heat Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.