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. 1,017 recalls have been distributed to Rhode Island in the last 12 months.
Showing 17201–17220 of 47,970 recalls
Recalled Item: Hand Sanitizer (Alcohol 80% v/v) topical solution Recalled by Ecolab Inc Due...
The Issue: Discoloration and Presence of Foreign Substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...
The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...
The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...
The Issue: Device did not meet the updated EUA packet requirements for positive percent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 9.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 7.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: Recalled by...
The Issue: A degradation defect was found that could lead to holes and donning tears at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare Recalled by RAYSEARCH LABORATORIES AB Due to When performing offline...
The Issue: When performing offline image review in RayCare 2C, RayCare 3A and RayCare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Dual Collapser Recalled by Sorin Group Italia S.r.l. Due to...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...
The Issue: LivaNova received complaints indicating the impossibility to collapse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.