Epidural Kit Correction: Medical Action Industries Issues Correction For Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
- Product
- Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
- Reason
- Medical Action Industries is correcting epidural kits containing recalled Huons Co. sodium chloride ampules.
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-09-10
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/f14c6615-f380-4140-939d-aaef5ca7a807