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. 1,059 recalls have been distributed to Maine in the last 12 months.
Showing 14441–14460 of 48,770 recalls
Recalled Item: ET82HP OUTLOOK PUMP EXTENSION SET-single-use for use with the Outlook...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Newborn Tray Recalled by ROi CPS LLC Due to Povidone-Iodine swabstick...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Core Biopsy Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REGARD Stereotactic Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...
The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outlook Pump Add-On Set-single use Recalled by B. Braun Medical, Inc. Due to...
The Issue: Leakage of the pump set within the cassette portion of the pump sets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....
The Issue: Through customer feedback, testing a sample with cardiac troponin I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...
The Issue: Incorrect version of labels were used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0 Recalled by...
The Issue: Due to a software defect that can intermittently cause the system to lock-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD Recalled by Medline...
The Issue: Potential for sterile barrier breach. Microscopic pinholes within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...
The Issue: Nonconforming product was distributed in error. Product was nonconforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...
The Issue: Labeling update concerning potential leaks from the catheter or the start-up...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.