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 26541–26560 of 47,970 recalls
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGB+ Multi Lumen Central Venous Catheterization Kit Recalled by Arrow...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous...
The Issue: These finished good kits may contain the incorrect Springwire Guide (SWG).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylphenidate Hydrochloride Tablets USP Recalled by Teva Pharmaceuticals...
The Issue: Failed Dissolution Specifications: Low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal Sterile Custom kits containing Medline Aplicare Povidone Iodine Prep...
The Issue: Custom surgical kits contain Aplicare Povidone Iodine Prep Pads which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fukuda Denshi patient monitor model DS-8100M and DS-8100N Product Usage:...
The Issue: For the Fukuda Denshi patient monitor model DS-8100, in less than 0.003%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...
The Issue: Labeling: Incorrect or Missing Package Insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...
The Issue: One reported complaint and discovered that the outer vial was out of round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...
The Issue: The label outside the cardboard box is labeled correctly but the pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ePHEDrine sulfate 50 mg/10 ml syringes in 0.9% Sodium Chloride Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.