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 25321–25340 of 27,456 recalls
Recalled Item: PadPro(R) Adult Radiotransparent Multifunction Electrodes Recalled by ConMed...
The Issue: ConMed was notified by the contract manufacturer that their wire/connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GII QuickAnchor Plus Recalled by Surgical Instrument Service And Savings,...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Average Medium Blade 9mm x 25mm x 0.38mm Ref. 2296-3-111 Lot 122590...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: - Cannulated Drill Bit for Mini TightRope Ref. AR-8911DC Lot Recalled by...
The Issue: The seal which maintains a sterile barrier for reprocessed medical devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical PerfOrma Anglographic Catheter 5F Multipack Product Usage:...
The Issue: Merit Medical Systems is recalling various lots of Performa Cardiac...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptex* Latex D Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens brand MicroScan Dried Negative Breakpoint Combo 47 panels...
The Issue: The product has the potential for false negative or delayed reaction for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streptex* kit Recalled by Remel Inc Due to The product may give weak or...
The Issue: The product may give weak or false negative test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medicals Epix¿ and Direct Drive Laparoscopic Graspers Recalled by...
The Issue: Applied Medical is conducting a voluntary recall on specific lot numbers of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes...
The Issue: BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMLC IV-ERGO Product Usage: Intended for use with rotating gantry Recalled...
The Issue: It is possible for an intermittent error to occur in the gantry sensor of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide Allergy. Sterile Allergy Treatment Syringe Tray. Recalled by...
The Issue: There has been an increase in complaints regarding the needle/safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421...
The Issue: Trans Warmer Infant and Transport Mattress not labeled with exp.date may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System disposable handpieces. Product Usage: The TX1...
The Issue: American Optisurgical, Inc. is recalling certain lots of TX1 Tissue Removal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Standard. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics VenaCure EVLT NeverTouch-FRS PROCEDURE KIT under the following...
The Issue: AngioDynamics Inc., is recalling Micro Introducer Kits and VenaCure EVLT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Breathe Medication Cup. For the delivery of liquid medications Recalled...
The Issue: Possible dislodgement of the "Plate A", if this instance occurs, it presents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar 360. Designed to meet the needs for lifting humans. Recalled by...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SlingBar Wide 670. Designed to meet the needs for lifting humans. Recalled...
The Issue: Retrospective review found 4 sling bars that may present a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.