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 27601–27620 of 47,970 recalls
Recalled Item: Ibuprofen Tablets Recalled by Time-Cap Laboratories, Inc. Due to Presence of...
The Issue: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...
The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100i Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp -...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution Recalled by Tris Pharma Inc. Due to Defective...
The Issue: Defective container: Oral solution leaking from container.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vis-U-All High Temp 4"x8" Heat Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 10"x15" Heat Seal Pouch 100 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 16"x16" Heat Seal Pouch 100 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 8"x10" Heat Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 3.5"x9" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 3.5"x22" Self Seal Pouch 200 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vis-U-All High Temp 13"x18" Self Seal Pouch 100 pouches per box Recalled by...
The Issue: On June 15, 2017, STERIS identified that the purple ink located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.