FDA recall record

JD & SN Inc., dba Moses Lake Professional HYDROXYPROGESTERONE CAPROATE OIL, injectable recall — FDA D-0100-2016

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

Class IIclassification
D-0100-2016official record ID
Nov 4, 2015report date

Recall record at a glance

Official recordD-0100-2016
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmJD & SN Inc., dba Moses Lake Professional Pharmacy
Report dateNov 4, 2015
Recall initiation dateJul 24, 2015
Quantity3 (4mL) syringes, 4 (5mL) syringes, 1 (6mL) syringe, 13 (10mL) syringes, 1 (16mL) syringe, 1 (18mL) syringe, 14 (20mL) syringes, 2 (22mL) syringes
LocationMoses Lake, WA, United States

Official product description

HYDROXYPROGESTERONE CAPROATE OIL, injectable Solution, 250 mg/mL, syringe sizes: 4 mL; 5 mL; 6 mL; 10 mL; 16 mL; 18 mL; 20 mL; and 22 mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Why the product was recalled

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

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.