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. 2,518 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,518 in last 12 months

Showing 1082110840 of 48,770 recalls

Medical DeviceSeptember 30, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BAUSCH + LOMB PHACO PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline received complaints on some of the breather pouches with in the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 30, 2022· Ingenus Pharmaceuticals Llc

Recalled Item: Flunisolide Nasal Solution Recalled by Ingenus Pharmaceuticals Llc Due to...

The Issue: Out of specification for related substances (impurities).

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· AuroMedics Pharma LLC

Recalled Item: Fondaparinux Sodium Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Subpotent Drug: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2022· VistaPharm, Inc.

Recalled Item: Pyridostigmine Bromide Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: cGMP Deviations: Out of specification for assay of one of the preservative...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 30, 2022· Swiss American Inc

Recalled Item: Saint Louis Domestic Brie Wedge Recalled by Swiss American Inc Due to...

The Issue: Potential contamination with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2022· CIPLA

Recalled Item: Arformoterol Tartrate Inhalation Solution Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility: environmental monitoring failure.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 29, 2022· Golden State Medical Supply Inc.

Recalled Item: Atenolol Tablets Recalled by Golden State Medical Supply Inc. Due to Label...

The Issue: Label Mix - up; a bottle labeled as Atenolol 25mg Tablets contained...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 29, 2022· Canon Medical System, USA, INC.

Recalled Item: Canon Aplio ultrasound system Recalled by Canon Medical System, USA, INC....

The Issue: After completion, ultrasound system's Stress Echo may not terminate if user...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· X-NAV Technologies, LLC

Recalled Item: X-Guide X-Mark Probe Tool -used for registering edentulous patients to...

The Issue: Product missing one of two welds connecting the tip to the shaft, if the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Kamiya Biomedical Company, LLC

Recalled Item: K-ASSAY IgA Immunoturbidimetric Assay Recalled by Kamiya Biomedical Company,...

The Issue: IgA Reagent may start showing cloudiness over time, which can affect assay...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· iRhythm Technologies, Inc.

Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...

The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Reusable Gel Pack Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...

The Issue: Users are being informed that the product should not be used on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2022· Covidien, LP

Recalled Item: Endo Stitch V-Loc PBT Non-Absorbable Reload Recalled by Covidien, LP Due to...

The Issue: Medtronic has received 210 reports of needles breaking during endoscopic...

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

Class II — Potential Health HazardOngoing