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. 2,496 recalls have been distributed to Rhode Island in the last 12 months.
Showing 11121–11140 of 27,456 recalls
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Trans-Ray 7Fr 40cc IAB...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible DCI Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexible Intubation Fiberscope Recalled by Karl Storz Endoscopy Due to...
The Issue: Updated sterilization instructions are being provided to ensure 1) a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Datascope Intra-Aortic Ballon Catheters (IABs)-Linear 7.5Fr 34cc IAB Kit...
The Issue: Potential Endotoxin Contamination
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Cannula HOLDEX Item # 450216 - Product Usage: - Recalled by C.A....
The Issue: Sample leaking from the sleeve covering the needle inside the cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The...
The Issue: The catalog ( REF ) number on the peelable inner labels (patient sticker)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista High Sensitivity Troponin I (TNIH) Flex reagent...
The Issue: Dimension Vista High Sensitivity Troponin I (TNIH) may exhibit a negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE SPECIALIZED ORTHOPEDICS Recalled by Nuvasive Specialized...
The Issue: During explantation, standard removal tools can generate sufficient forces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DABRA RA-308 Excimer Laser Recalled by Ra Medical Systems, Inc. Due to Due...
The Issue: Due to the taller wheel mounting on the laser, the laser may fall over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM Recalled...
The Issue: The connector linking the EtCO2 module to the HemoBox may break and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product...
The Issue: Thermo Scientific" Remel" Bordetella pertussis Agglutinating Serum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POLARSTEM COLLAR Reamer Guide Recalled by Smith & Nephew Orthopaedics AG Due...
The Issue: Multiple lots being recalled due to a product design issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Software Version R1.0 and R1.1 Recalled by Philips Medical...
The Issue: Philips has become aware of a software issue, where the kV and mA values are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra x5 1-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...
The Issue: The electrode insulating material on the Cobra EMG ET tube used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame Recalled by...
The Issue: Modular Junction Box (MJB) cables can melt and affect the bed functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube Recalled by...
The Issue: The electrode insulating material on the Cobra EMG ET tube used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Recalled by...
The Issue: May have one or more dimensional features out of tolerance includes: thread...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra x5 1-CH EMG ET Tube Recalled by Neurovision Medical Products Inc Due...
The Issue: The electrode insulating material on the Cobra EMG ET tube used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ezycare Face Mask Recalled by BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA...
The Issue: Disposable face masks labeled as non-medical were distributed to customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobra x5 2-Ch EMG ET Tube Recalled by Neurovision Medical Products Inc Due...
The Issue: The electrode insulating material on the Cobra EMG ET tube used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.