FDA Drug recall D-0067-2016

CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only…

FDA Drug
Class II
terminated
Published 2015-11-04

On 2015-11-04 the FDA classified a Class II recall of CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, Rx only… by Jd And Sn, citing lack of Assurance of Sterility; all sterile human compounded drugs within expiry.

Read the official FDA Drug notice

Agency	FDA Drug
Recall number	D-0067-2016
Classification	Class II
Status	terminated
Initiated	2015-07-24
Published	2015-11-04
Last updated	2026-09-13 11:51 UTC
Company	Jd And Sn
Distribution	US

Product

CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 175 UNITS/0.175ML per syringe, packaged in 14, 26, and 40-count containers, 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	01052015@18, 01072015@12, 01122015@13, 01142015@7, 01192015@18, 01212015@16, 01262015@11, 02022015@13, 02192015@10, 022… 01052015@18, 01072015@12, 01122015@13, 01142015@7, 01192015@18, 01212015@16, 01262015@11, 02022015@13, 02192015@10, 02232015@22, 03042015@20, 03092015@46, 03162015@13, 03182015@17, 03252015@23, 03302015@13, 04012015@11, 04152015@14, 04212015@15, 04272015@13, 05062015@19, 05112015@27, 05202015@16, 05272015@29, 06032015@19, 06102015@27, 06152015@31, 06172015@40, 06222015@27, 06292015@27, 07012015@12, 07062015@16, 07092014@4, 07152015@13, 07162014@3, 07212014@4, 07232014@15, 07282014@14, 07302014@5, 08112014@19, 08182014@7, 08252014@14, 09022014@22, 09152014@10, 09172014@16, 09222014@6, 09292014@22, 10062014@15, 10132014@20, 10222014@14, 10272014@13, 11032014@17, 11052014@19, 11262014@13, 12302014@8, t03022015@10, t04072015@32, t05112015@26, t05152015@4, t07132015@6.

code_info

01052015@18, 01072015@12, 01122015@13, 01142015@7, 01192015@18, 01212015@16, 01262015@11, 02022015@13, 02192015@10, 022…

01052015@18, 01072015@12, 01122015@13, 01142015@7, 01192015@18, 01212015@16, 01262015@11, 02022015@13, 02192015@10, 02232015@22, 03042015@20, 03092015@46, 03162015@13, 03182015@17, 03252015@23, 03302015@13, 04012015@11, 04152015@14, 04212015@15, 04272015@13, 05062015@19, 05112015@27, 05202015@16, 05272015@29, 06032015@19, 06102015@27, 06152015@31, 06172015@40, 06222015@27, 06292015@27, 07012015@12, 07062015@16, 07092014@4, 07152015@13, 07162014@3, 07212014@4, 07232014@15, 07282014@14, 07302014@5, 08112014@19, 08182014@7, 08252014@14, 09022014@22, 09152014@10, 09172014@16, 09222014@6, 09292014@22, 10062014@15, 10132014@20, 10222014@14, 10272014@13, 11032014@17, 11052014@19, 11262014@13, 12302014@8, t03022015@10, t04072015@32, t05112015@26, t05152015@4, t07132015@6.

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-0067-2016%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.