FDA Drugs recall ·
PHENYLephrine added to 0.9% sodium chloride, 40 mg/250 mL* (160 mcg/mL)… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0272-2025
- Date
- (initiated February 20, 2025)
- Company / brand
- Central Admixture Pharmacy Services, Inc.
6580 Snowdrift Rd Ste 100, Allentown, PA, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 1546 bags
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
PHENYLephrine 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.
Why was it recalled?
Presence of Particulate Matter
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot 37-928390, Exp Date, 03MAR2025; Lot 37-928796, Exp Date, 09MAR2025; Lot 37-928839, Exp Date, 10MAR2025
Distribution
Product was distributed nationwide within the United States
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0272-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.