La Vita Compounding Pharmacy, LLC recalls Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Recall notice
Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.
Contact the company & request your remedy
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We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
Source Page by GovInfoNow · govinfonow.com/recall/40403-la-vita-compounding-pharmacy-llc-recalls-methyl-folate-ca-1mg · Recall date June 25, 2018 · FDA enforcement record: FDA #D-0922-2018
Cite this page
“La Vita Compounding Pharmacy, LLC recalls Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la.” GovInfoNow, recall dated June 25, 2018. https://govinfonow.com/recall/40403-la-vita-compounding-pharmacy-llc-recalls-methyl-folate-ca-1mg. Based on FDA recall #D-0922-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0922-2018%22&limit=1).
How to tell if you have this one
- Brand
La Vita Compounding Pharmacy, LLC- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Product was distributed to patients via patient specific prescription only in CA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0921-2018 | Methylcobalamin 1mg/mL Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), packaged in 10 mL and 30 mL vials, Rx only, la VITA Compounding Pharmacy, 858.453.2500; Lot #s: 139140@3, Exp 07/23/2018; 141106@1, Exp 08/21/2018; 142919@13, Exp 09/17/2018; 143291@6, Exp 09/23/2018; 145701@3, Exp 10/29/2018; 146932@3, Exp 11/19/2018 | 19,040 mL total dispensed in 10 mL and 30 mL vials |
| 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 Pharmacy, 858.453.2500; Lot #: 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 | 17,610 mL total dispensed in 10 mL and 30 mL vials |
| D-0923-2018 | Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2500; Lot #: 144326@3, Exp 07/10/2018; 145953@2, Exp 08/05/2018 | 191 vials |
Contact La Vita Compounding Pharmacy, LLC
We’ve drafted a message you can send La Vita Compounding Pharmacy, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0922-2018 — La Vita Compounding Pharmacy, LLC La Vita Compounding Pharmacy, LLC recalls Methyl Folate CA+ 1mg/m Hello, I own a La Vita Compounding Pharmacy, LLC recalls Methyl Folate CA+ 1mg/ml Injection w/Pres. (Benzyl Alcohol 1% in Sterile Water), 10 mL and 30 mL vials, Rx only, la that is covered by recall D-0922-2018 from La Vita Compounding Pharmacy, LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0922-2018 (June 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0922-2018 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.