FDA recall record

Fagron Compounding Services LLC dba Fagron Succinylcholine Chloride, 100 mg per 5mL, 20 mg recall — FDA D-0946-2017

Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier

Class IIclassification
D-0946-2017official record ID
Jul 12, 2017report date

Recall record at a glance

Official recordD-0946-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFagron Compounding Services LLC dba Fagron Sterile Services
Report dateJul 12, 2017
Recall initiation dateJun 19, 2017
Quantity1,056 5mL syringes
LocationWichita, KS, United States

Official product description

Succinylcholine Chloride, 100 mg per 5mL, 20 mg per mL syringe. IV Use Only. JCB Laboratories, 8710 E 34th St., N. Wichita, KS 67226 UPC 7335968405

Why the product was recalled

Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial supplier

Distribution information

Nationwide in the USA

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: Letter.

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.