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. 1,017 recalls have been distributed to Rhode Island in the last 12 months.
Showing 17481–17500 of 47,970 recalls
Recalled Item: 11 IN(28cm)APPX 0.97ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112 IN(284cm) APPX 14.6ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.32 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold Recalled by ICU...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Appx 16.6 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...
The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) -...
The Issue: Breaking at the point of a welded joint
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...
The Issue: Insufficient amount of antibody without an error message or alarm
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...
The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by Granules...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minoxidil/Biotin/Spironolactone 1.25/5/25mg capsules Recalled by MasterPharm...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.