PF-Succinylcholine Chloride Injection recall: Labeling Error
PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B…
Why was PF-Succinylcholine Chloride Injection recalled?
Incorrect labeling: Incorrect or missing lot and/or exp date
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?
Lots: SU9079A, SU9079B, Exp 4/5/2020
- Product
- PF-Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL), Rx Only, Single-Dose Container, 5 x 10 mL pre-filled syringes, Nephron 503B…
- Recalling firm
- Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center
- Quantity
- 19,390 syringes
- Distribution
- Nationwide in the U.S.
- Recall date
- November 6, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)