RecallRadar

FDA Drug recall D-0111-2016

PAPAVERINE/PHENTOLAMINE, Injectable Solution, 30MG/1MG/ML, 10 mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555…

On 2015-11-04 the FDA classified a Class II recall of PAPAVERINE/PHENTOLAMINE, Injectable Solution, 30MG/1MG/ML, 10 mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555… by Jd And Sn, citing lack of Assurance of Sterility; all sterile human compounded drugs within expiry.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0111-2016
ClassificationClass II
Statusterminated
Initiated2015-07-24
Published2015-11-04
Last updated2026-09-13 11:51 UTC
CompanyJd And Sn
DistributionUS

Product

PAPAVERINE/PHENTOLAMINE, Injectable Solution, 30MG/1MG/ML, 10 mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Reason

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

Identifiers

code_infot09172014@29, t08252014@1, t06082015@10, t03032015@26, t02272015@23, t01232015@12, t01122015@36, t05132015@15

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0111-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.