Home › Device types › OGE
Epidural Anesthesia Kit
FDA product code OGE · Class 2 · Anesthesiology
2,411
Registered devices
1,130
Adverse events
33
Recalls
0
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCDesign Options® — B. BRAUN MEDICAL INC.Design Options® — B. BRAUN MEDICAL INC.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCDesign Options® — B. BRAUN MEDICAL INC.CARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Design Options® — B. BRAUN MEDICAL INC.NA — PAJUNK MEDICAL SYSTEMS, LPCARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Design Options® — B. BRAUN MEDICAL INC.CARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Perifix® — B. BRAUN MEDICAL INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-17 | Windstone Medical Packaging, Inc. | Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HC |
| 2026-04-10 | Medline Industries, LP | Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, incl |
| 2026-03-19 | Medline Industries, LP | During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market |
| 2026-01-29 | B Braun Medical Inc | B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due |
| 2026-01-29 | B Braun Medical Inc | B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due |
| 2026-01-29 | B Braun Medical Inc | B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due |
| 2026-01-29 | B Braun Medical Inc | B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary recall due |
| 2025-09-18 | B BRAUN MEDICAL INC | Potential for the lid of the catheter connector to be in the incorrect position. |
| 2025-09-18 | B BRAUN MEDICAL INC | Potential for the lid of the catheter connector to be in the incorrect position. |
| 2025-09-18 | B BRAUN MEDICAL INC | Potential for the lid of the catheter connector to be in the incorrect position. |
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