Recall Register

Drug recall: PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy…

Class I FDA enforcement event 96307. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Presence of Particulate Matter

Class I, in the words of FDA

a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death

Central Admixture Pharmacy Services, Inc. started this drug recall on 20 Feb 2025. The firm address in the FDA record is in Allentown, PA. FDA put the recall in Class I. FDA event 96307 has 1 product record. The first FDA enforcement report date is 19 Mar 2025. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Product was distributed nationwide within the United States

Recalling firm

Central Admixture Pharmacy Services, Inc., Allentown, PA.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 96307: product records
Recall numberProductQuantityClassStatusReport date
D-0272-2025PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL), Rx Only, CAPS, Central Admixture Pharmacy Services, Inc., 6580 Snowdrift Rd., Ste 100, Allentown, PA 18106, 855-275-2270, NDC 71285-6092-1.1546 bagsClass IOngoing19 Mar 2025

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Drug events that started in 2025
322
Share of these events in Class I
9%
Product records in this event
1Median of the firm: 32
Events of the firm on the register
10

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 96307. https://recallregister.com/fda/i/96307/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA drug enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Product was distributed nationwide within the United States
What quantity of product is in FDA event 96307?
The FDA record gives this quantity: 1546 bags
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many drug recalls of 2025 have the same class?
9% of the 322 drug events that started in 2025 are in Class I.