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. 2,455 recalls have been distributed to Maine in the last 12 months.
Showing 15661–15680 of 27,655 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: Five warning statements are missing from the instructions for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Vitamin D total II Recalled by Roche Diagnostics Corporation Due to...
The Issue: The device may give a falsely elevated result that is non-reproducible. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT540. The systems are intended for head Recalled by GE...
The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX VATS1SCDX DO ZABIEGOW VATS Product Usage: The Endo GIA Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm(...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX 01KBAR006116V PROC BYPASS 01KBAR0061(Item Code 01KBAR006116V PROC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)KIT4184 APEN LOBECTOMY KIT X0 Item Number: KIT4184 APEN LOBECTOMY...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143 Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX MGBGLOGX1 ZESTAW MINI GASTRIC BYPASS Product Usage: The Endo Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.