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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 23121–23140 of 48,770 recalls
Recalled Item: Various GE Magnetic Resonance System on-site software version Product Usage:...
The Issue: Possible incorrect software version loaded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSet XT Injectable HA Bone Cement Recalled by Howmedica Osteonics Corp....
The Issue: Incorrect expiry date of 9-Feb-20 Correct expiry date is 30-Aug-19
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot LA 20 () The Staclot¿ LA and Staclot¿ Recalled by Diagnostica Stago,...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow CVC 2 Lumen Recalled by Arrow International Inc Due to The lidstock...
The Issue: The lidstock states the incorrect priming volume and flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Staclot¿ LA () The Staclot¿ LA and Staclot¿ LA Recalled by Diagnostica...
The Issue: There have been reports of shortened (T1-T2) results, where some instances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quetiapine Tablets USP 400 mg Recalled by Ascend Laboratories LLC Due to...
The Issue: Presence of Foreign Substance; metal shard found in tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDS Light Suspension Recalled by Stryker Communications Due to There is a...
The Issue: There is a potential the joint in the suspension of the device is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Systems Software Version 9.01 Update Kit. Recalled by bioMerieux,...
The Issue: The VITEK¿ 2 Systems Software Version 9.01 software may display incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to Isocenter shifts...
The Issue: Isocenter shifts when using dose tracking in RayStation 3.5, RayStation 4.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empower FastLoad CT Syringe Pack -sterile disposable syringe kit for...
The Issue: Insufficient seal on the sterile barrier of the device, compromising the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion Pack Recalled by LivaNova USA Due to 4-way stopcocks and stopcock...
The Issue: 4-way stopcocks and stopcock manifold assembled in certain perfusion tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by AMERICAN...
The Issue: Cross contamination with other products: This sub-recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bucky Stand SU-4000 Input 2017.11.17. SU41711085 Date: 2017-11-17 Recalled...
The Issue: Unintentional U-Arm movement
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz. Recalled by...
The Issue: One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / Recalled...
The Issue: Possible contamination with cleaning chemicals.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Volcano FFR software used in the following systems connected...
The Issue: Interoperability issue that affects certain systems that use the recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stationary Fluoroscopic X-ray System CombiDiagnost R90 Recalled by Philips...
The Issue: kV/mA lockin not functioning as specified which may result in the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clopidogrel Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Out-of-Specification results were observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.