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. 2,363 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,363 in last 12 months

Showing 2372123740 of 27,456 recalls

Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Weck¿ Vista" Recalled by Teleflex Medical Due to Complaints were received of...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 10mm Weck¿ Vista" Cannula-only 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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port  Short Length (53mm)...

The Issue: Complaints were received of leakage of insufflation gas through the device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port  Long 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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: 12mm Weck¿ Vista" Cannula-only 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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Deknatel Teleflex Medical Silk Black Braided Silk Suture Nonabsorbable...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Teleflex Medical Recalled by Teleflex Medical Due to Product does not meet...

The Issue: Product does not meet minimum needle attachment strength requirements; thus,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing