CLASS II Drug recall · Reported 7 Mar 2018 · FDA Enforcement Report

SyrSpend SF Suspending Base, a) recalled by Fagron

Fagron is recalling SyrSpend SF Suspending Base, a) (, distributed nationwide in the US. The recall was initiated on 14 Feb 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesa) 17I28-U80-039976, exp. 10/02/2020; b) 17I28-U80-039977, exp. 10/02/2020
Quantity recalleda) 1007 bottles (500 mL) and b) 738 bottles (4 L)

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-0547-2018
FDA event ID
79253
Recalling firm
Fagron, Saint Paul, MN
Classification
Class II
Status
Terminated
Recall initiated
14 Feb 2018
FDA classified
27 Feb 2018
Reported
7 Mar 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Mold

Timeline

14 Feb 2018Recall initiated by company
27 Feb 2018Classified by FDA+13 days
7 Mar 2018Published in enforcement report+8 days

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

Reason for recall

Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).

Product as listed by the FDA

SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120

Where it was distributed

Nationwide, USA

Nationwide

Questions about this recall

Why was it recalled?

Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).

Which lots are affected?

a) 17I28-U80-039976, exp. 10/02/2020; b) 17I28-U80-039977, exp. 10/02/2020

Where was it sold?

Nationwide, 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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

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