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. 2,520 recalls have been distributed to Maine in the last 12 months.
Showing 9281–9300 of 27,655 recalls
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to There is the potential...
The Issue: There is the potential bacterial including Nontuberculous mycobacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas infinity central lab running software version 3.01.03 through 3.02.08...
The Issue: Under specific circumstances created by the user, the cobas e flow test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST IMIPENEM RELEBACTAM. in vitro diagnostic Recalled by Biomerieux Inc...
The Issue: Major errors (Resistant result instead of Susceptible result) were observed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EJM4011 Jamshidi Evolve" Bone Marrow Biopsy/Aspiration Needle with Specimen...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kaluza C Flow Cytometry Software Versions: 1.0* Recalled by Beckman Coulter,...
The Issue: Software anomalies that may lead to the generation of erroneous results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x...
The Issue: Due to complaints received regarding incomplete/open packaging seals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Sonicision Reusable Generator-converts electrical power from the...
The Issue: Potential for a manufacturing assembly error-may result in a non-functional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYLA software. Used to manage microbiology test workflow from the Recalled...
The Issue: Software anomaly - Under certain conditions, unwanted alterations to results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: muRata Vios Monitoring System Model 2050 Recalled by Murata Vios, Inc. Due...
The Issue: During the set-up and workflow to begin Vios monitoring, it has been noticed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Configura Advance Chair Recalled by Accora Inc Due to The firm has...
The Issue: The firm has identified a potential for the backrest to become detached from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe 1 Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.