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.

52,535 total recalls
2,858 in last 12 months

Showing 87618780 of 29,093 recalls

Medical DeviceDecember 22, 2021· Medtronic Xomed, Inc.

Recalled Item: NIM TRIVANTAGE EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due...

The Issue: There is potential for multiple issues due to a manufacturing nonconformity.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Avanos Medical, Inc.

Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors -...

The Issue: The External Retention Bolster contained in the kit may be a larger diameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Synthes (USA) Products LLC

Recalled Item: Universal Chuck-The Universal Chuck is an Instrument Handle provided as...

The Issue: Top cap may loosen and detach if the Universal Chuck becomes jammed and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Avanos Medical, Inc.

Recalled Item: MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL Recalled by...

The Issue: The External Retention Bolster contained in the kit may be a larger diameter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2021· Empowered Diagnostics LLC

Recalled Item: ImmunoPass Recalled by Empowered Diagnostics LLC Due to COVID test kits were...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2021· Empowered Diagnostics LLC

Recalled Item: CovClear COVID-19 Rapid Antigen Test Recalled by Empowered Diagnostics LLC...

The Issue: COVID test kits were offered for sale and distributed to consumers in the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 21, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant Recalled by Medtronic Vascular, Inc. Due to Stent Graft Systems...

The Issue: Stent Graft Systems built with specific batches of taper tip assemblies have...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2021· Vyaire Medical

Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to Potential...

The Issue: Potential cessation in ventilation can occur under specific conditions.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 20, 2021· Canon Medical System, USA, INC.

Recalled Item: Flat Panel Detector Recalled by Canon Medical System, USA, INC. Due to...

The Issue: Abnormal images such as horizontal stripes may be displayed and recovery may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Nobel Biocare Usa Llc

Recalled Item: NobelReplace Conical Connection RP 4.3x11.5 mm STERILE R Recalled by Nobel...

The Issue: Due to 16 complaints related to drivers not engaging in implants. According...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2021· Covidien Llc

Recalled Item: Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm Recalled by Covidien...

The Issue: The firm has received six (6) complaint reports from customers indicating...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2021· Draeger Medical, Inc.

Recalled Item: Draeger Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due...

The Issue: 26 Fabius MRI Anesthesia machines were distributed with internal hoses...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20545 Vitale Silver calcium Alginate Dressings 4x5 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20522 Vitale Silver calcium Alginate Dressings 2x2 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20500 Vitale Silver calcium Alginate Dressing Ropes Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20544 Vitale Silver calcium Alginate Dressings 4x4 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2021· CellEra LLC

Recalled Item: 20548 Vitale Silver calcium Alginate Dressings 4x8 Recalled by CellEra LLC...

The Issue: Firm discovered that an incorrect version of the Instructions for Use (IFU)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 14, 2021· Smith & Nephew, Inc.

Recalled Item: Acufex Access Advanced Positioning Kit - indicated for use to Recalled by...

The Issue: Products were shipped to the Global Distribution Center instead of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2021· Abiomed, Inc.

Recalled Item: OXY-1 System Recalled by Abiomed, Inc. Due to The firm has received...

The Issue: The firm has received complaints of the OXY-1 System Console experiencing a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 13, 2021· Collagen Matrix, Inc.

Recalled Item: DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches...

The Issue: Outer packaging (outer pouch) is not sealed compromising sterility and...

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

Class II — Potential Health HazardOngoing