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. 2,332 recalls have been distributed to Rhode Island in the last 12 months.
Showing 34881–34900 of 47,970 recalls
Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...
The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xanax (alprazolam) tablets Recalled by Pfizer Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Airways Development LLC WaterPAP Positive Airway Pressure Device #WP-7700....
The Issue: Airways Development LLC has received a complaint about a canister leaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shorts on The Beach Strong Formula by Pink Bikini capsules Recalled by...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pink Bikini Strong Formula capsules Recalled by Lucy's Weight Loss (dba....
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shorts on The Beach Golden Edition by Pink Bikini Recalled by Lucy's Weight...
The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HARMONIC ACE+ 7 Laparoscopic Shears with Advanced Hemostasis (23cm Recalled...
The Issue: Complaints of holes in Tyvek which can compromise the sterile barrier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is Recalled by...
The Issue: During the use of the TELETOM Series 4 & 6 there is potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets...
The Issue: Cross Contamination With Other Products: Potential cross-contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...
The Issue: Users can merge a device import file with an image study that already has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELITech Clinical Systems reagents used on the Selectra ProS and Recalled by...
The Issue: ELITech Clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 100 system included the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Envoy 500 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon 300 system includes the following product numbers and Recalled by...
The Issue: ELITech clinical Systems reagents based on Trinder reaction used on the Eon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sentinel MULTIGENT Ammonia Ultra Reagent Recalled by Sentinel CH SpA Due to...
The Issue: Results for ammonia are below the linear range of the assay for samples that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baby Omega 3 Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baby Vitamin D Dietary supplement (in liquid form) Recalled by Zarbee's...
The Issue: Some units of each lot may contain contaminants (elevated aerobic plate...
Recommended Action: Do not consume. Return to store for a refund or discard.