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. 2,524 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,524 in last 12 months

Showing 77417760 of 27,655 recalls

Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Due to a software...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam AXL Wave . Used to image the anterior segment of the eye. Recalled...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2022· Oculus Optikgeraete GMBH

Recalled Item: Pentacam HR . Used to image the anterior segment of the eye. Recalled by...

The Issue: Due to a software issue, IOL calculator printout often does not accurately...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2022· Olympus Corporation of the Americas

Recalled Item: ShockPulse-SE Lithotripsy Generator Model/Serial: SPL-S Recalled by Olympus...

The Issue: Mis-wired component-the improperly wired component can result in additional...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2022· Zap Surgical Systems

Recalled Item: ZAP-X Radiosurgery System Recalled by Zap Surgical Systems Due to Software...

The Issue: Software issue identified in cases of initial patient setup with large...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 0.5ml Code: OT005 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 1ml Reusable Low Dose Enteral Syringe Code: LHE01LD Recalled...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 2.5ml Code: OT25 Recalled by Medicina Uk Ltd Due...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina ENFit 5ml Reusable Enteral Syringe Code: LHE05 Recalled by Medicina...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 5ml Code: OTH05 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Oral Tip Syringe 1ml Code: OT01 Recalled by Medicina Uk Ltd Due to...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 2.5ml Code: OTH25 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2022· Medicina Uk Ltd

Recalled Item: Medicina Reusable Oral syringe 1ml Code: OTH01 Recalled by Medicina Uk Ltd...

The Issue: Plunger component has been manufactured with an unapproved material...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci S/Si Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2022· Intuitive Surgical, Inc.

Recalled Item: Da Vinci X/Xi Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Due to the potential for unexpected motion caused by the partial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2022· Micro Therapeutics, Inc.

Recalled Item: Echelon -14 Recalled by Micro Therapeutics, Inc. Due to Outer carton...

The Issue: Outer carton packaging of microcatheters were exposed to wet substance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2022· Micro Therapeutics, Inc.

Recalled Item: Echelon -14 Micro Catheter Recalled by Micro Therapeutics, Inc. Due to Outer...

The Issue: Outer carton packaging of microcatheters were exposed to wet substance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· OrthoPediatrics Corp

Recalled Item: Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN...

The Issue: Manufacturing variance near transition of tip is increasing the likelihood...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Biosense Webster, Inc.

Recalled Item: CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath Recalled by Biosense...

The Issue: Outside packaging for a device indicated for introducing cardiovascular...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2022· Trinity Sterile, Inc.

Recalled Item: Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708...

The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing