Home › Device types › OGJ
Nerve Block Tray
FDA product code OGJ · Class 2 · Anesthesiology
3,258
Registered devices
74
Adverse events
45
Recalls
0
510(k) clearances
Devices with this code
Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCDesign Options® — B. BRAUN MEDICAL INC.CUSTOM HEALTHCARE SYSTEMS, INC — Manus Medical, LLCCARDINAL HEALTH — Cardinal Health 200, LLCPediatric Lumbar Puncture Tray — ARGON MEDICAL DEVICES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCDesign Options® — B. BRAUN MEDICAL INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCBusse Hospital Disposables — ROBERT BUSSE & CO., INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.Design Options® — B. BRAUN MEDICAL INC.Medline Industries, Inc. — MEDLINE INDUSTRIES, INC.CARDINAL HEALTH — Cardinal Health 200, LLCMedline Industries, Inc. — MEDLINE INDUSTRIES, INC.Medical Action Industries — MEDICAL ACTION INDUSTRIES INC.Aligned Medical Solutions — Aligned Medical SolutionsCARDINAL HEALTH — Cardinal Health 200, LLCCONTIPLEX® — B. BRAUN MEDICAL 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 |
| 2026-05-21 | Medline Industries, LP | The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocai |
| 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 |
| 2026-02-27 | Medline Industries, LP | Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result i |
| 2026-02-25 | Medline Industries, LP | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2026-01-07 | Medline Industries, LP | Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated ster |
| 2025-03-03 | MEDLINE INDUSTRIES, LP - Northfield | There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits. |
| 2024-10-16 | MEDLINE INDUSTRIES, LP - Northfield | The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position. |
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