CLASS III Drug recall · Reported 25 Apr 2018 · FDA Enforcement Report

Vasopressin added to 0.9% Sodium Chloride Injection USP per mL) recalled

Pharmedium Services is recalling Vasopressin added to 0.9% Sodium Chloride Injection USP per mL), distributed in Massachusetts, Washington. The recall was initiated on 10 Apr 2018 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot: 180660057S Exp. 6/5/2018
Quantity recalled72 bags

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-0632-2018
FDA event ID
79799
Recalling firm
Pharmedium Services, Lake Forest, IL
Classification
Class III
Status
Terminated
Recall initiated
10 Apr 2018
FDA classified
17 Apr 2018
Reported
25 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone

Timeline

10 Apr 2018Recall initiated by company
17 Apr 2018Classified by FDA+7 days
25 Apr 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

cGMP deviations

Product as listed by the FDA

Vasopressin 50 Units added to 250 mL 0.9% Sodium Chloride Injection USP (0.2 units per mL), Rx only, PharMEDium Services, LLC 12620 W. Airport Blvd #130 Sugar Land, TX 77478

Where it was distributed

MA, WA

MassachusettsWashington

Questions about this recall

Why was it recalled?

cGMP deviations

Which lots are affected?

Lot: 180660057S Exp. 6/5/2018

Where was it sold?

MA, WA

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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