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Epidural Anesthesia Kit

FDA product code OGE · Class 2 · Anesthesiology

2,456
Registered devices
1,145
Adverse events
34
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-06-17Windstone Medical Packaging, Inc.Windstone Medical Packaging recalled specific items and lots of AMS convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices
2026-04-10Medline Industries, LPMedline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, incl
2026-03-19Medline Industries, LPDuring an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due
2026-01-29B Braun Medical IncB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due
2026-01-15Custom Interventional Pain Management, LLCDue to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.
2025-09-18B BRAUN MEDICAL INCPotential for the lid of the catheter connector to be in the incorrect position.
2025-09-18B BRAUN MEDICAL INCPotential for the lid of the catheter connector to be in the incorrect position.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.