FDA recall record

OurPharma fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% recall — FDA 99837

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the…

Not Yet Classifiedclassification
99837official record ID
Sep 16, 2026report date

Recall record at a glance

Official record99837
CategoryDrug Recalls
ClassificationNot Yet Classified
FDA record statusOngoing
Recalling firmOurPharma LLC
Report dateSep 16, 2026
Recall initiation dateSep 3, 2026
Quantity1,610 bags
LocationFayetteville, AR, United States

Official product description

fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City Lake, Fayetteville, AR, NDC 73013-1013-01.

Why the product was recalled

Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Distribution information

Nationwide within the U.S

How to read the classification

The classification “Not Yet Classified” is reproduced from the official source record. Refer to the FDA record for the agency’s current classification and instructions.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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