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. 1,119 recalls have been distributed to Maryland in the last 12 months.
Showing 8761–8780 of 29,093 recalls
Recalled Item: JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250 Recalled by...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DREAMTOME 49-20MM/450CM Material Number: M00584020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-450-035 Material Number: M00573030 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAGTOME RX 49-30-260-035 Material Number: M00573020 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRATOME RX 44-30MM/260CM Material Number: M00583050 Recalled by Boston...
The Issue: Sterility of device is compromised due to a sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.