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Drug recall · FDA · Published August 10, 2017

Premier Pharmacy Labs Inc recalls Neostigmine Methylsulfate (single dose syringe) 1 mg per mL 5 mg per 5 mL Injectable Hospital/Office Use Only

Stability Date Doesn't Support Expiry: labeling error indicating a beyond use date that exceeds current stability data.

🇺🇸 FDA recall #D-0129-2018DrugPremier Pharmacy Labs Inc ›
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Recalling firmPremier Pharmacy Labs Inc8265 Commercial Way · Weeki Wachee, FL 34613-4511
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
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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/41402-premier-pharmacy-labs-inc-recalls-neostigmine-methylsulfate-single-dose-syringe · Recall date August 10, 2017 · FDA enforcement record: FDA #D-0129-2018

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“Premier Pharmacy Labs Inc recalls Neostigmine Methylsulfate (single dose syringe) 1 mg per mL 5 mg per 5 mL Injectable Hospital/Office Use Only.” GovInfoNow, recall dated August 10, 2017. https://govinfonow.com/recall/41402-premier-pharmacy-labs-inc-recalls-neostigmine-methylsulfate-single-dose-syringe. Based on FDA recall #D-0129-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0129-2018%22&limit=1).

How to tell if you have this one

  • Brand
    Premier Pharmacy Labs Inc
  • Category
    Drug
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Contact Premier Pharmacy Labs Inc

We’ve drafted a message you can send Premier Pharmacy Labs Inc to request your refund or repair — edit it as you like.

Subject: Recall D-0129-2018 — Premier Pharmacy Labs Inc Premier Pharmacy Labs Inc recalls Neostigmine Methylsulfate (single dose 

Hello,

I own a Premier Pharmacy Labs Inc recalls Neostigmine Methylsulfate (single dose syringe) 1 mg per mL 5 mg per 5 mL Injectable Hospital/Office Use Only that is covered by recall D-0129-2018 from Premier Pharmacy Labs Inc.

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-0129-2018 (August 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0129-2018 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA