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. 2,800 recalls have been distributed to Maryland in the last 12 months.
Showing 15061–15080 of 29,093 recalls
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...
The Issue: Due to a manufacturing variation in the arm that can result in a persistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Ferritin Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i TSH Reagent Kit Recalled by Abbott Ireland Diagnostics Division...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Progesterone Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Total Beta-hCG Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Estradiol Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Free T4 Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i 25-OH Vitamin D Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model...
The Issue: HVAD Battery Charger units manufactured with wrong inductors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireSR Recalled by LivaNova USA Inc Due to This...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics VNS Therapy AspireHC Model 105 Generator Recalled by LivaNova USA...
The Issue: This recall is an expansion of Z-3019-2017 and Z-3020-2017, which was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2 Recalled by LivaNova USA...
The Issue: This recall is being initiated due to reports that that the therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LivaNova VNS Therapy System Recalled by LivaNova USA Inc Due to Lead...
The Issue: Lead impedance values reported by the affected VNS generator will be higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare 9805 and 9805P Hydraulic Patient Lifts Recalled by Invacare...
The Issue: Invacare has identified via customer complaints, the potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revanesse Versa Recalled by Prollenium Medical Technologies Inc. Due to...
The Issue: Labeling error. The product is labeled with an 18 month expiration date,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.