Product Recalls in Rhode Island
Product recalls affecting Rhode Island — including food, drugs, consumer products, medical devices, and vehicles distributed to Rhode Island. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,521 recalls have been distributed to Rhode Island in the last 12 months.
Showing 9261–9280 of 27,456 recalls
Recalled Item: Exactech Connexion GXL acetabular polyethylene liners used in the following...
The Issue: Risk of edge-loading and premature prosthesis wear is possible in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MY01 Continuous Compartmental Pressure Monitor Recalled by MY01, INC. Due to...
The Issue: There is an incorrect version of the needle in the introducer part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Anatomic Shoulder System for the following Part Numbers: 1....
The Issue: Complaints have been received concerning the humeral stem failing to mate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KeyPrint Soft- bottle Recalled by Straumann USA LLC Due to Product label...
The Issue: Product label intended for the European community was distributed to the USA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUTTING ELECTRODE BIPO 24.5FR Recalled by Richard Wolf GmbH Due to Product...
The Issue: Product labeled as Cutting Electrode may contain BIVAP electrode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.