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. 1,762 recalls have been distributed to Rhode Island in the last 12 months.
Showing 32041–32060 of 47,970 recalls
Recalled Item: Zenostar MT Color Impulse orange Recalled by Ivoclar Vivadent, Inc. Due to...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color A1 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenostar MT Color A2 60ml Recalled by Ivoclar Vivadent, Inc. Due to The...
The Issue: The primary packaging of these products may show leaks in individual cases....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Domaine de Provence Neutral 3"¿ Cone Tart Shells Produced Exclusively...
The Issue: Product contains undeclared allergen, coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Remeven Cream Recalled by Stratus Pharmaceuticals Inc Due to...
The Issue: Crystallization; Complaints that cream appears to have crystallized
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM -...
The Issue: Subpotent Drug: Out of Specification assay values on stability for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Centaur XPT system software versions V1.0.1 (Bundle 1.0.912 SMN...
The Issue: Eight (8) issues were identified which may affect the results generated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONLINE TDM Vancomycin 100 tests Recalled by Roche Diagnostics Operations,...
The Issue: Roche Diagnostics Operations, Inc. has issued a voluntary recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novation Press-Fit Splined RDD Recalled by Exactech, Inc. Due to Labeled...
The Issue: Labeled with the incorrect Global Trade Item Number (GTIN). The GTIN on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HK FEMORAL ASSEMBLY Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The surface inside of the femoral component, where cement is applied for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Model 882482 Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Upgrade Model 882454 Recalled by Philips Medical Systems...
The Issue: The firm became aware of an issue where during a non-Auto Body Contouring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iConnect Access software. The firm name on the label is Merge Healthcare...
The Issue: Software displayed incorrect prior reports in the viewport area, only when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External...
The Issue: LIFEPAK CR Plus Automated External Defibrillators (AED) or LIFEPAK EXPRESS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.