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. 2,560 recalls have been distributed to Rhode Island in the last 12 months.

47,970 total recalls
2,560 in last 12 months

Showing 22612280 of 47,970 recalls

Medical DeviceMay 19, 2025· Limacorporate S.p.A

Recalled Item: PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW Recalled by Limacorporate S.p.A Due...

The Issue: There is the potential that the eccentrical adaptor with screw, black laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2025· Limacorporate S.p.A

Recalled Item: PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW .15.702 Recalled by Limacorporate...

The Issue: There is the potential that the eccentrical adaptor with screw, black laser...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2025· Drs Vascular, Inc

Recalled Item: Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog...

The Issue: XXX

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

Class II — Potential Health HazardOngoing
DrugMay 15, 2025· Amerisource Health Services LLC

Recalled Item: Indomethacin Extended-Release Capsules Recalled by Amerisource Health...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Theophylline (Anhydrous) Extended-Release Tablets Recalled by Glenmark...

The Issue: OOS results reported for the Dissolution (by UV) test.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 15, 2025· CareFusion 213, LLC

Recalled Item: BD ChloraPrep Clear Recalled by CareFusion 213, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: The affected product may exhibit an open...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline UMBILICAL TRAY W/3.5&5FR CATH Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: There is a possible packaging defect impacting the outer Tyvec pouch that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2025· SunMed Holdings, LLC

Recalled Item: Broselow Pediatric Emergency Rainbow Tape (distribution by AirLife) Recalled...

The Issue: The impacted tape was manufactured with incorrect information on the tape....

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 15, 2025· Contamac Solutions, Inc.

Recalled Item: Contamac Recalled by Contamac Solutions, Inc. Due to Contact lens insertion...

The Issue: Contact lens insertion solution may lack sterility.

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

Class II — Potential Health HazardOngoing
DrugMay 14, 2025· AsttraZeneca Pharmaceuticals LP

Recalled Item: Airsupra (albuterol and budesonide) inhalation aerosol Recalled by...

The Issue: Defective delivery system

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: FEM-FLEX II Product Name: Femoral Arterial Cannula Model/Catalog...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: FEM-FLEXII Product Name: Femoral Arterial Cannula Model/Catalog...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2025· Edwards Lifesciences, LLC

Recalled Item: Brand Name: Optisite Arterial Cannula Product Name: Optisite Arterial...

The Issue: due to complaints received for 3mm to 4mm section wire exposed/protruding...

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

Class I — Serious Health HazardOngoing
DrugMay 13, 2025· AvKARE

Recalled Item: Celecoxib Capsules Recalled by AvKARE Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: manufacturer recalled because one...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension Recalled by Zydus...

The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 13, 2025· Belmont Instrument LLC

Recalled Item: Allon 2001. Part Number: 200-00263 Recalled by Belmont Instrument LLC Due to...

The Issue: An investigation into a report of the patient wrap (ThermoWrap), used with...

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

Class II — Potential Health HazardOngoing