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 16741–16760 of 27,456 recalls
Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...
The Issue: The instruments are not able to pass instrument verification which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SORIN GROUP Recalled by Sorin Group USA, Inc. Due to Medtronic informed...
The Issue: Medtronic informed LivaNova that some of their DLP Pressure Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System Recalled by...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVADAQ SPY-PHI Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to The...
The Issue: The sterile drape material may contain a pinhole compromising its integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc....
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/ Aspiration Tray with Biopsy Needle...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Deluxe Bone Marrow Biopsy/Aspiration Tray Recalled by Robert Busse &...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse Hospital...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomcat Instrument Recalled by Hologic, Inc Due to A Tomcat Instrument...
The Issue: A Tomcat Instrument software anomaly that causes the pipettor arm to make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Tiburon(R) Arthroscopy Drape Recalled by Cardinal Health 200,...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumbar Puncture Tray Recalled by Robert Busse & Co. Inc. d.b.a. Busse...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Converters(R) Under Buttocks Drape with Fluid Control Pouch II Recalled by...
The Issue: Outer label of some units of product number/lot number 8482, Lot 16LFS235...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety-Deluxe Basic Soft Tissue Biopsy Tray without Biopsy Needle Recalled...
The Issue: BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt MV Bone Cement 40GM Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.