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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 3188131900 of 48,770 recalls

Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x picture archiving and communication system Syngo.x is a software...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Polypropylene Surgical Sutures Recalled by Riverpoint Medical, LLC Due to...

The Issue: Polypropylene Surgical Sutures are recalled because the seals may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam and Symbia E gamma camera systems with patient beds Recalled by...

The Issue: "We have received reports of patients hair being caught in the e.cam and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Medtronic Inc.

Recalled Item: CareLink iPro Version 1.10 Recalled by Medtronic Inc. Due to Medtronic...

The Issue: Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via picture archiving and communication system Syngo via is a Recalled...

The Issue: Software error. Incorrect values for the volume calculation from a freehand...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2016· Riverpoint Medical, LLC

Recalled Item: Nylon Surgical Suture for human use and vet use Recalled by Riverpoint...

The Issue: Nylon Surgical Sutures are recalled because the seals may become open during...

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

Class II — Potential Health HazardOngoing
DrugAugust 5, 2016· Teva North America

Recalled Item: Claravis (isotretinoin capsules USP) Recalled by Teva North America Due to...

The Issue: Failed Impurities/Degradation Specifications.

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Amerisource Health Services

Recalled Item: buPROPion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed dissolution specifications - the out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Bupivacaine Hydrochloride Inj. Recalled by Hospira Inc., A Pfizer Company...

The Issue: Presence of particulate matter: Confirmed customer report for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 4, 2016· Genzyme Corporation / Genzyme Biosurgery

Recalled Item: Mozobil (plerixafor injection) 24 mg/1.2 mL (20 mg/mL) per vial Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
FoodAugust 4, 2016· Ricker Hill Orchards

Recalled Item: Ricker Hill Orchards Cran-Breeze Recalled by Ricker Hill Orchards Due to...

The Issue: Product contains patulin at levels higher than the FDA established limit of...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 4, 2016· Ricker Hill Orchards

Recalled Item: Apple Cider: Ricker Hill Orchards Apple Cider 1/2 GAL (64 FL OZ) 1.89 LITERS...

The Issue: Product contains patulin at levels higher than the FDA established limit of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 4, 2016· Terumo Medical Corp

Recalled Item: MISAGO RX Self Expanding Peripheral Stem Recalled by Terumo Medical Corp Due...

The Issue: During recent routine testing, the MISAGO Peripheral Stent was found not to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2016· Beckman Coulter Inc.

Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...

The Issue: Beckman Coulter is recalling the UniCel DxH Slidemaker Stainer Coulter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome without LeMills Recalled by LeMaitre...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· LeMaitre Vascular, Inc.

Recalled Item: 1.5 mm HYDRO LeMaitre Valvulotome Recalled by LeMaitre Vascular, Inc. Due to...

The Issue: Wire which deploys the loop may be come detached at the handle causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ 70cc Piston Syringe with Catheter Tip Recalled by C.R. Bard, Inc. Due...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Piston Syringe Recalled by C.R. Bard, Inc. Due to Package Defect:...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARDIA¿ 60cc Piston Irrigation Syringe Recalled by C.R. Bard, Inc. Due to...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2016· C.R. Bard, Inc.

Recalled Item: BARD¿ Irrigation Recalled by C.R. Bard, Inc. Due to Package Defect: Products...

The Issue: Package Defect: Products may be at risk for having a slit defect on the...

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

Class II — Potential Health HazardOngoing