Mckesson Medical Surgical recalls hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only,
Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
Recall notice
Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
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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/41821-mckesson-medical-surgical-recalls-hydralazine-hydrochloride-injection-usp-20-mg · Recall date March 8, 2017 · FDA enforcement record: FDA #D-0668-2017
Cite this page
“Mckesson Medical Surgical recalls hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only,.” GovInfoNow, recall dated March 8, 2017. https://govinfonow.com/recall/41821-mckesson-medical-surgical-recalls-hydralazine-hydrochloride-injection-usp-20-mg. Based on FDA recall #D-0668-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0668-2017%22&limit=1).
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Contact Mckesson Medical Surgical
We’ve drafted a message you can send Mckesson Medical Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-0668-2017 — Mckesson Medical Surgical Mckesson Medical Surgical recalls hydrALAZINE HYDROCHLORIDE INJECTION, US Hello, I own a Mckesson Medical Surgical recalls hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only, that is covered by recall D-0668-2017 from Mckesson Medical Surgical. 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-0668-2017 (March 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0668-2017 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.