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. 2,858 recalls have been distributed to Maryland in the last 12 months.
Showing 9121–9140 of 29,093 recalls
Recalled Item: REF/Catalogue Number GSXE0030B Recalled by W L Gore & Associates, Inc. Due...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0020 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSX0030A Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REF/Catalogue Number GSXE0025 Recalled by W L Gore & Associates, Inc. Due to...
The Issue: Septal Occluders contain the incorrect expiration date. Product is labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA Versions: 4.7 Recalled by BioMerieux SA Due to Under certain...
The Issue: Under certain conditions, there is a risk for a false negative result.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m Recalled by Abbott...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization Recalled by...
The Issue: There is a potential for false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic sterile single-use blades that are components of the StraightShot...
The Issue: There was an increase in complaints related to tip breaks and wobble/vibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force with software syngo.CT VB20 Model #10742326 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge with software syngo.CT VB20 Model #10590000 Recalled...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS with software syngo.CT VB20 Model #8098027 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash with software syngo.CT VB20 Model #10430603...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Confidence with software syngo.CT VB20 Model #10590100 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Drive with software syngo.CT VB20 Model #10431700 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Edge Plus with software syngo.CT VB20 Model #10267000 Recalled by...
The Issue: software syngo.CT VB20 in the installed base, with or without syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.