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. 2,864 recalls have been distributed to Maryland in the last 12 months.

52,535 total recalls
2,864 in last 12 months

Showing 64216440 of 29,093 recalls

Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· GE OEC Medical Systems, Inc

Recalled Item: OEC 9800 Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...

The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· GE OEC Medical Systems, Inc

Recalled Item: OEC Elite Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...

The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· NeuMoDx Molecular Inc

Recalled Item: NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of...

The Issue: Potential for lot number discrepancies between the test strip packaging and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMay 12, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline O.R. Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: The scissors were manufactured without a tip protector resulting in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Ossur H / F

Recalled Item: Icelock 125 Ratchet Recalled by Ossur H / F Due to A mechanical lock used to...

The Issue: A mechanical lock used to connect and release a locking liner into a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Boston Scientific Neuromodulation Corporation

Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...

The Issue: Pending update to indirect decompression system instructions for use...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing