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 17521–17540 of 47,970 recalls
Recalled Item: Yohimbine HCL 5.4mg Capsule Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone 50 mg Modified Release Capsule Recalled by MasterPharm LLC Due...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Plus 1.25mg Capsule Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Modified Release 100 mg Capsule Recalled by MasterPharm LLC Due...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone 300 mg Troche Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone (Modified Release) 150 mg Capsule Recalled by MasterPharm LLC...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone (Rapid-Dissolve) 150 mg Tablet Recalled by MasterPharm LLC Due...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tadalafil 7 mg Capsule Recalled by MasterPharm LLC Due to Lack of Processing...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hostess Raspberry Zingers Recalled by Hostess Brands, LLC Due to Product...
The Issue: Product potentially has mold prior to best by date.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 6' (15 cm) Appx 0.09 ml Recalled by ICU Medical, Inc. Due to Incorrect...
The Issue: Incorrect filter assemblies in IV administration set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial)...
The Issue: Microbial contamination of non-sterile products: positive microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidothol Patch Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Auto ID Module Model 8600 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 - Product Usage: is intended Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PCA Module Model 8120 - Product Usage: is intended Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Syringe Module Model 8110 - Product Usage: is intended Recalled by...
The Issue: LED display, which provides infusion or patient monitoring values, on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.