Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,562 recalls have been distributed to Maine in the last 12 months.
Showing 501–520 of 27,655 recalls
Recalled Item: Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with...
The Issue: IFU and device kit labeling contains misleading statements leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Reaction Vessels Recalled by Beckman Coulter, Inc. Due to It has...
The Issue: It has been determined that certain lots of Access 2 Reaction Vessels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris" Pump Module model 8100 UDI-DI code: 10885403810046 The Recalled...
The Issue: Due to a number of modules flashed with a date and time associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard InLay Optima Size: 6 Fr. x 14 cm Recalled by C.R. Bard Inc Due to...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm Recalled by C.R....
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe-T-Centesis 6 Fr Catheter Drainage Tray Recalled by Bard Peripheral...
The Issue: Acute drainage catheters, indicated for use in removing fluid during acute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm Recalled by C.R. Bard...
The Issue: Labeling discrepancy; Ureteral stent actual size may not match the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100425-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100225-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100220-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100325-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100125-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Diasol Product Name: 100230-10-DEX100 Recalled by Diasol, Inc...
The Issue: Safety and efficacy of dialysis acid concentrate cannot be assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Activated Clotting Time Low-Range Test Cuvette Recalled by Accriva...
The Issue: Test cuvettes, used with an assay for monitoring heparin anticoagulation,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.