RecallRadar

FDA Drug recall D-0065-2016

CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL

On 2015-11-04 the FDA classified a Class II recall of CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL 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-0065-2016
ClassificationClass II
Statusterminated
Initiated2015-07-24
Published2015-11-04
Last updated2026-09-13 11:51 UTC
CompanyJd And Sn
DistributionUS

Product

CHORIONIC GONADOTROPIN, Injectable Solution, 5000 UNITS/0.1 mL, vial sizes: 5 mL; 6 mL; 8 mL; 10 mL, 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_info
t12292014@35, t12192014@15, t12162014@29, t10232014@24, t09162014@29, t09032014@6, t07252014@16, t07142015@6, t07022015…t12292014@35, t12192014@15, t12162014@29, t10232014@24, t09162014@29, t09032014@6, t07252014@16, t07142015@6, t07022015@8, t06152015@32, t05272015@33, t04282015@11, t04162015@34, t04092015@8, t04022015@30, t02262015@24, t02032015@21, and t01232015@10

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-0065-2016%22

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