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.

47,970 total recalls
2,298 in last 12 months

Showing 4124141260 of 47,970 recalls

DrugMarch 14, 2014· Shire Human Genetic Therapies, Inc.

Recalled Item: VPRIV¿ (velaglucerase alfa for injection) Recalled by Shire Human Genetic...

The Issue: Presence of Particulate Matter; Particulates identified as stainless steel...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: All Natural Recalled by Smiley National Inc Due to Smiley National is...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Enhanced Maeng Da Leaf Powder Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Enhanced Bali Leaf Powder Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 14, 2014· Smiley National Inc

Recalled Item: Natural Bali Kratom 40 Recalled by Smiley National Inc Due to Smiley...

The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2014· Breg Inc

Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...

The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2014· Pain Free By Nature

Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 13, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...

The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2014· Merit Medical Systems, Inc.

Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...

The Issue: The products are labeled as sterile but were not sterilized.

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

Class II — Potential Health HazardOngoing
DrugMarch 11, 2014· Paddock Laboratories, LLC

Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...

The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: IntelliSpace Portal (ISP) Recalled by Philips Medical Systems (Cleveland)...

The Issue: During SPECT reconstructions using Attenuation Correction and Scatter...

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 Stainless Steel 2 (metric 5) Monofilament...

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: 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
Medical DeviceMarch 11, 2014· Teleflex Medical

Recalled Item: Nonabsorbable Surgical Suture Recalled by Teleflex Medical Due to Product...

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: Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture...

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