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. 2,366 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,366 in last 12 months

Showing 2692126940 of 48,770 recalls

FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Basil Garlic Organic Polenta Recalled by San Gennaro Foods, Inc Due to Date...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
FoodOctober 13, 2017· San Gennaro Foods, Inc

Recalled Item: Traditional Organic Polenta Recalled by San Gennaro Foods, Inc Due to Date...

The Issue: Date coding ink was being printed directly on the food contact surface of...

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

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2017· Genzyme Corporation

Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...

The Issue: Labeling: Incorrect or Missing Package Insert.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...

The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Dental Inc

Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...

The Issue: The device may contain a manufacturing condition affecting the geometry of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2017· Zimmer Biomet, Inc.

Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...

The Issue: Gamma sterilization validation testing indicates the sterilization dose for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Karl Storz Endoscopy

Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...

The Issue: The label outside the cardboard box is labeled correctly but the pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...

The Issue: One reported complaint and discovered that the outer vial was out of round...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2017· Crimson Trace Corporation

Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...

The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Magnesium sulfate 10 Gm added to Lactated Ringer's 250 mL bags Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Midazolam HCL 100 mg (1mg/mL) 100 mL Cassette in 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Diltiazem HCL 125 mg added to 0.9% Sodium Chloride 100 ml bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Norepinephrine Bitartrate16 mg added to 0.9% Sodium Chloride 250 mL bag...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: Succinylcholine 200 mg/10 mL Syringe Recalled by Banner Pharmacy Services,...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: fentanyl citrate (PF) 1100 mcg (20 mcg/mL) 55 mL syringes Recalled by Banner...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2017· Banner Pharmacy Services, LLC

Recalled Item: OXYtocin 30 units added to 0.9% Sodium Chloride 500 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund