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. 2,544 recalls have been distributed to Rhode Island in the last 12 months.
Showing 4081–4100 of 47,970 recalls
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thiamine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 750 mg per 250 mL 0.9% Sodium Chloride Injection USP Recalled...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP Recalled by...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP Recalled by...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...
The Issue: CGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack...
The Issue: Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: intelliPATH Universal HRP Detection Kit Recalled by Biocare Medical, LLC Due...
The Issue: Kits containing the DAB chromogen buffer, intended for use in either manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Nivagen Pharmaceuticals Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.