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. 2,351 recalls have been distributed to Rhode Island in the last 12 months.
Showing 25561–25580 of 27,456 recalls
Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...
The Issue: The recall was initiated because Shimadzu Corporation has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: Pump shutting off during use without warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...
The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...
The Issue: There was an occurrence where the patient case data did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...
The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...
The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrea¿ CT Brain Perfusion made available in various configurations under...
The Issue: Vital Images, Inc. (Vital Images) received one report about potential user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...
The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...
The Issue: The Column rotation can accidentally be moved to a different position which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...
The Issue: Two unsealed pouches were found at an Edwards' distribution location in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.