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. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 9381–9400 of 27,655 recalls
Recalled Item: Edwards Recalled by Edwards Lifesciences, LLC Due to There is a potential...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...
The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...
The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...
The Issue: Potential for mold contamination (Aspergillus vadensis)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...
The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...
The Issue: The MRI system contains a component that does not meet the appropriate flame...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...
The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.