CLASS I Drug recall · Reported 11 Jul 2018 · FDA Enforcement Report

Neostigmine Methylsulfate Injection Solution, 5 mg recalled

Fagron Compounding Services is recalling Neostigmine Methylsulfate Injection Solution, 5 mg per, 1 mg per mL prefilled syringe, 5, distributed nationwide in the US. The recall was initiated on 29 Jun 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #: C274-000004690, BUD: 09/21/18.
Quantity recalled840 prefilled syringes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0910-2018
FDA event ID
80383
Recalling firm
Fagron Compounding Services, Wichita, KS
Classification
Class I
Status
Terminated
Recall initiated
29 Jun 2018
FDA classified
6 Jul 2018
Reported
11 Jul 2018
Type
Voluntary: Firm initiated
Reason category
Labeling Errors

Timeline

29 Jun 2018Recall initiated by company
6 Jul 2018Classified by FDA+7 days
11 Jul 2018Published in enforcement report+5 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.

Product as listed by the FDA

Neostigmine Methylsulfate Injection Solution, 5 mg per 5 mL, 1 mg per mL, 5 mL prefilled syringe, 5 syringes per package, Rx only, Fagron Sterile Services, ICB Laboratories, 8710 E 34th St. N., Wichita, KS 67205, NDC 71266-2003-02.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.

Which lots are affected?

Lot #: C274-000004690, BUD: 09/21/18.

Where was it sold?

Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 80383

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