PlainRecalls
FDA Drug Moderate Class II Terminated

Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01

Reported: September 22, 2021 Initiated: August 19, 2021 #D-0794-2021

Product Description

Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01

Reason for Recall

Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle

Details

Units Affected
55,344/100 count bottles
Distribution
Product was distributed nationwide.
Location
Coventry, RI

Frequently Asked Questions

What product was recalled?
Oxycodone Hydrochloride Tablets, USP, 10 mg, 100 count bottle, Rx only, Marketed by: Rhodes Pharmaceuticals L.P., Coventry RI 02816, Manufactured by: Purdue Pharma L.P., Stanford, CT 06901 NDC 42858-002-01. Recalled by Rhodes Pharmaceuticals, L.P.. Units affected: 55,344/100 count bottles.
Why was this product recalled?
Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Which agency issued this recall?
This recall was issued by the FDA Drug on September 22, 2021. Severity: Moderate. Recall number: D-0794-2021.