RecallRadar

FDA Drug recall D-0922-2018

Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharma…

On 2018-07-25 the FDA classified a Class II recall of Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharma… by La Vita Compounding Pharmacy, citing lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0922-2018
ClassificationClass II
Statusterminated
Initiated2018-06-25
Published2018-07-25
Last updated2026-09-13 11:52 UTC
CompanyLa Vita Compounding Pharmacy
DistributionCA

Product

Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharmacy, 858.453.2500

Reason

Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.

Identifiers

code_infoLot #: 140089@1, Exp 08/06/2018; 141968@6, Exp 09/03/2018; 143381@2, Exp 09/24/2018; 145265@13, Exp 10/22/2018; 146479@6, Exp 11/12/2018

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0922-2018%22

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