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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 20981–21000 of 27,655 recalls
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...
The Issue: It was identified by a customer complaint that some I.V. poles were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...
The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...
The Issue: A component on the systems power board can fail in a manner which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: miraDry System consisting of the MD4000-MC Console Recalled by Miramar Labs,...
The Issue: Update to labeling for the miraDry Console to remind users to only use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the SmartSite Extension Set due to disconnection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry XPT Systems Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Multiple Software issues. Auto Start-UP Fail, Calibration Interval Resets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed Recalled by...
The Issue: Hill-Rom is voluntarily recalling the Hill-Rom 100 Low Bed due to complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helioseal F Sealant 1 x 1.25 g Recalled by Ivoclar A. G. Due to A defect...
The Issue: A defect occurred in the production process of Helioseal F Sealant; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Threaded Plate Holder- Long for 3.5mm Locking Hold Recalled by...
The Issue: The affected part number and lot listed above is incorrectly etched with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antibacterial Hydro Personal Catheter Recalled by C.R. Bard, Inc. Due to...
The Issue: Incorrect unit labeling. The case label and shelf box are correct, Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.