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. 2,298 recalls have been distributed to Rhode Island in the last 12 months.
Showing 41281–41300 of 47,970 recalls
Recalled Item: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS Recalled by...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Universal Cannula Recalled by Teleflex Medical Due...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may containin a syringe...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA...
The Issue: Some 23 kHz Torque Wrenches were incorrectly assembled and contained a 36...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine HCl Extended-Release Capsules Recalled by Greenstone Llc Due to...
The Issue: Presence of Foreign Tablets/Capsules: report of a foreign capsule with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Effexor XR (venlafaxine HCl) Extended-Release Capsules Recalled by Pfizer Us...
The Issue: Presence of Foreign Tablets/Capsules: A Pharmacist reported that a bottle of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.