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. 2,882 recalls have been distributed to Maryland in the last 12 months.
Showing 3681–3700 of 29,093 recalls
Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FM Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 500 Series Ventilators (Description/REF): PURITAN BENNETT...
The Issue: Any single affected ventilator should only be used for the 10- year labelled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK MINI CR-4HH-P Recalled by CareFusion 303, Inc. Due to Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-2FH-2FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-4FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P Recalled by CareFusion 303, Inc. Due...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-14HH-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P Recalled by CareFusion 303, Inc....
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P Recalled by CareFusion 303, Inc. Due to...
The Issue: Due to software issue, there is a potential when a restock label is printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with...
The Issue: Potential for false negative response on the NIM Vital Nerve Monitoring System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...
The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...
The Issue: Specimen collection device may leak after the patient sample swabs have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...
The Issue: Potential for defective test cartridges which may result in false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to There is a...
The Issue: There is a risk that alarms will not be received by the Arial Wireless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Call Station Recalled by Securitas Healthcare LLC Due to This is a...
The Issue: This is a risk that alarms will not be received by the Arial Wireless Nurse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: If blood culture identification panel is used in conjunction with specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.