Fentanyl recall
Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205
Why was Fentanyl recalled?
Subpotency: Out-of-specification stability test result for low potency was obtained.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 1220021578, Exp 12/2/2020; 1220021732, Exp 12/9/2020; 1220022385, Exp 12/29/2020; 1220022582, Exp 1/6/2021
- Product
- Fentanyl, 250 mcg/ 5mL, Injection for IV or IM use, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct., Little Rock, AR 72205
- Recalling firm
- SCA Pharmaceuticals
- Quantity
- 4,843 syringes
- Distribution
- Product was distributed to three hospitals in MO & LA.
- Recall date
- December 23, 2020
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)