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. 1,610 recalls have been distributed to Maine in the last 12 months.
Showing 3181–3200 of 48,770 recalls
Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...
The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...
The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...
The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...
The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Single Use Guide Sheath Kits with the following product Recalled by...
The Issue: Potential for the radiopaque tip of the guide sheath component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Sertera Biopsy Device Product Name: Sertera Biopsy Device...
The Issue: Devices presented a condition in which the inner needle separated from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device Recalled by...
The Issue: Error in the IFU lists an incorrect incubation time on one occasion of 20...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Central Station. Model Number: MS26800 The Infinity CentralStation...
The Issue: Edifier speakers (shipped in or after April 2023) may not annunciate when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: Possibility of the patient falling from the table related to the mattress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C System Code: (1) 722001 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 Recalled...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 System Code: (1) 722038 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Catalog (1) 722003 (2) 722010 (3)722026 Recalled by PHILIPS...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M12 System Code: (1) 722227 (2) 722231 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXperFD20/15 System Code: (1) 722058 Recalled by PHILIPS MEDICAL...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 Recalled by...
The Issue: Potential safety issue with the AD7 and AD7X patient tables (both tilt and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.