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 18661–18680 of 52,535 recalls
Recalled Item: OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails Recalled by Merete...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur)...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...
The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.