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. 2,515 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,515 in last 12 months

Showing 1176111780 of 48,770 recalls

Medical DeviceJune 2, 2022· Surgical Innovations Ltd

Recalled Item: YelloPort Elite Universal Seal. For use in laparoscopic procedures. Recalled...

The Issue: There is the potential that YelloPort Elite Universal Seals packaging may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Breas Medical, Inc.

Recalled Item: Vivo 45LS Ventilator- intended to provide continuous or intermittent...

The Issue: A forced shutdown of one of the processors did not generate a watch dog...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Wright Medical Technology, Inc.

Recalled Item: Stryker INFINITY Resect Guide for INBONE Talus Recalled by Wright Medical...

The Issue: The instrument is incorrectly color coded.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD.

Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...

The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Skytron, Div. The KMW Group, Inc

Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...

The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...

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

Class II — Potential Health HazardOngoing
FoodJune 1, 2022· Taylor Farms Retail Inc

Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...

The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...

The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...

The Issue: An issue with propagation of treatment course information from RayStation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Spectranetics Corporation

Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to The...

The Issue: The LAS-100 Laser system may detect an inoperable hardware component during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ultradent Products, Inc.

Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...

The Issue: SE primer may be missing some or all of the resin portion of the chemistry....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...

The Issue: The product was potentially exposed to below-recommended storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Software related alarm escalation defect occurs after approximately 25 days...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Boston Scientific Corporation

Recalled Item: GreenLight HPSEA Laser Fibers Recalled by Boston Scientific Corporation Due...

The Issue: Several complaints were received for the affected lot; users received a...

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

Class III — Low RiskOngoing
Medical DeviceMay 31, 2022· Baxter Healthcare Corporation

Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...

The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Ossur Americas

Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...

The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Avance CS2 Recalled by GE Healthcare, LLC Due to The base of...

The Issue: The base of the anesthesia system can have a crack and could potentially...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2022· Fruselva America SPA

Recalled Item: Nature s Promise Organic Mango Recalled by Fruselva America SPA Due to...

The Issue: Elevated levels of thallium (heavy metal)

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund