CLASS III Drug recall · Reported 20 Jan 2021 · FDA Enforcement Report
Succinylcholine Chloride PF Inj recalled by US Compounding
US Compounding is recalling Succinylcholine Chloride PF Inj, distributed nationwide in the US. The recall was initiated on 16 Dec 2020 and the FDA has classified it as Class III.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0223-2021
- FDA event ID
- 86997
- Recalling firm
- US Compounding, Conway, AR
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 16 Dec 2020
- FDA classified
- 11 Jan 2021
- Reported
- 20 Jan 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Drug class
- Compounded Drugs
Timeline
| 16 Dec 2020 | Recall initiated by company | |
| 11 Jan 2021 | Classified by FDA | +26 days |
| 20 Jan 2021 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrect position on the product label making it illegible.
Product as listed by the FDA
Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes, Rx only, US Compounding, 1270 Don's Lane, Conway, AR 72032
Where it was distributed
USA Nationwide
Questions about this recall
Is Succinylcholine Chloride PF Inj recalled?
Yes. US Compounding recalled Succinylcholine Chloride PF Inj on 16 Dec 2020. The recall is Class III and its status is Terminated. Recall number D-0223-2021.
Why was it recalled?
Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrect position on the product label making it illegible.
Which lots are affected?
Lot #: 20202010@6 BUD: 02/17/2021
Where was it sold?
USA Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from US Compounding
All 65| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Neostigmine Methylsulfate PF Inj recalled by US Compounding | US Compounding | Labeling Errors | Nationwide |
| Drug | CLASS II | Ephedrine Sulfate, 50 mg/ Single Use Syringe recalled by US Compounding | US Compounding | Sterility | Nationwide |
| Drug | CLASS II | LET Gel 4% (Lidocaine HCl 4% + EPINEPHrine HCl 05% + recalled | US Compounding | Other | Nationwide |
| Drug | CLASS I | Docusate Oral 10 mg/mL Oral Syringe recalled by US Compounding | US Compounding | Sterility | TX |
| Drug | CLASS II | Fentanyl PF (25 mcg/mL) Single Use Syringe, For IV recalled | US Compounding | Sterility | Nationwide |