CLASS II Drug recall · Reported 26 Jul 2023 · FDA Enforcement Report

PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride IV Bag recalled

New England Life Care is recalling PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride IV Bag @60 Total volume), distributed nationwide in the US. The recall was initiated on 10 Jul 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 20230524-6FBB77, Exp 21OCT2023
Quantity recalled82 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-0927-2023
FDA event ID
92690
Recalling firm
New England Life Care, Woburn, MA
Classification
Class II
Status
Terminated
Recall initiated
10 Jul 2023
FDA classified
19 Jul 2023
Reported
26 Jul 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

10 Jul 2023Recall initiated by company
19 Jul 2023Classified by FDA+9 days
26 Jul 2023Published in enforcement report+7 days

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

Reason for recall

CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.

Product as listed by the FDA

PHENYLephrine HCl 10mg added to 0.9% Sodium Chloride 250mL, 250 mL IV Bag @60 Total volume), RX only, Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, MA 01801-1042, NDC: 71546-450-25;

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.

Which lots are affected?

Lot # 20230524-6FBB77, Exp 21OCT2023

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 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.

Other products in this recall event

3 other products · FDA event 92690

This product is part of a recall event; the main page for the event is Vancomycin HCl added to 0.9% Sodium Chloride IV Bag recalled.

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