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. 2,269 recalls have been distributed to Rhode Island in the last 12 months.
Showing 43761–43780 of 47,970 recalls
Recalled Item: CMC Saddle Product Usage: The Ascension CMC is intended to Recalled by...
The Issue: As a result of a quality review, labelling content discrepancies were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prempro (Conjugated Estrogen/Medroxyprogesterone Acetate) tablets 0.625...
The Issue: Failed Dissolution Specifications: Pfizer Inc. (Pfizer) is recalling PREMPRO...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...
The Issue: Failed Dissolution Specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Uncle Eddies Vegan Oatmeal Chocolate Cookies Recalled by International...
The Issue: International Desserts of Glendale, California is recalling Uncle Eddies...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Synthes 2.4mm VA-LCP Two Column Volar Distal Radius Plate and Recalled by...
The Issue: The firm is initiating a Field Safety Correction for the labeling of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Vector Distractor Pin Holding Clamp Recalled by Synthes USA HQ, Inc....
The Issue: Synthes is initiating a voluntary Medical Device removal for specified part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX Instrument Recalled by Becton Dickinson & Co. Due to Electrical power...
The Issue: Electrical power module installed on some in vitro diagnostic instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharmalucence Kit for the Preparation of Technetium Tc 99m Sestamibi...
The Issue: Presence of Particulate Matter; particulate found in retain samples
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin Recalled by Sandoz Incorporated Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Sandoz Inc is recalling Cefazolin for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fudge Buttercream Frosted Peanut Butter cookies Recalled by Cheryls Due to...
The Issue: Undeclared allergen due to use of incorrect packaging on peanut butter cookies.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker Oasys Midline Occiput Plate-1) Small 2) Medium 3) Large Recalled by...
The Issue: Stryker has received reports from customers indicating post-operative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TotalCare Bed used with AccuMax Quantum VPC mattress AccuMax Quantum...
The Issue: When the bed is put into the chair egress position, the magnets on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO-MED ORTHO TOTAL JOINT TRACECART(R) Recalled by DeRoyal Industries Inc...
The Issue: DeRoyal recalled kits that contained Stryker togas which were recalled for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******QTY 1***APEX Arthroscopy Tubing Set. Intended for use for Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by...
The Issue: Conmed Linvatec received complaints that their products C7120 APEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle¿ Destination¿ Peripheral Guiding Sheath Recalled by Terumo Medical...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Glidesheath (tm) Recalled by Terumo Medical Corporation Due to...
The Issue: Medical devices were incorrectly labeled with extended expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glutathione 200 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acepromazine 25 mg/ml Injection Recalled by Lowlite Investments, Inc. D/B/A...
The Issue: Lack of Assurance of Sterility: FDA inspection findings resulted in concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.