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. 2,882 recalls have been distributed to Maryland in the last 12 months.
Showing 4161–4180 of 29,093 recalls
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes labeled as: a) SYR 10ML L/L CONTROL Recalled by MEDLINE INDUSTRIES,...
The Issue: These syringes were identified to be affected by the FDA Safety Alert issued...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...
The Issue: Potential holes and tears in the sterile packaging (header bag) of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optical Inspection System Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yamaha Surface Mounter YR series Recalled by YAMAHA MOTOR CORPORATION Due to...
The Issue: Non-medical laser products which were determined to not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc....
The Issue: The guide tip can become damaged and result in the tip detaching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in....
The Issue: Potential contamination of the product with latex adhesive residual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelli-C: Right side suspended Tabletop Recalled by NRT X-RAY A/S Due to...
The Issue: X-ray system C-arm may experience uncontrolled motion if 1) AC motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT VR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.