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. 2,447 recalls have been distributed to Rhode Island in the last 12 months.
Showing 16641–16660 of 27,456 recalls
Recalled Item: 94" (239 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126" (320 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 121" (307 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 117" (297 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lopez Valve¿ Recalled by ICU Medical, Inc. Due to Some devices were labeled...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 94" (239 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139" (353 cm) Y-Type Blood Set w/ 170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 32" (81 cm) Appx 4.4 mL Blood Set w/20 Drop 200 Micron Filter Recalled by...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Brainlab AG Due to Risk of unintended...
The Issue: Risk of unintended motion while the AIRO system is in transport mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8000 Modular Series system Recalled by Roche Diagnostics Corporation...
The Issue: A software failure may incorrectly set the system settings to "default"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Clip for Oracle Retractor Recalled by Synthes (USA) Products LLC Due...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Torque Limiting Handle. Must be used with supplemental...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.