Halyard CPT PEDS ADULT CH PACK - Medical convenience kits recallZ-0433-2025 · AVID Medical, Inc. · initiated Sep 20, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from AVID Medical, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
FDA root cause category: Process control
What the company is doing
Avid Medical issued Urgent: Voluntary Medical Device Recall letter via email on 9/20/24. Letter states reason for recall, health risk and action to take: If you received any of the batches/lots identified in APPENDIX 1, please review your inventory, and discard the entire kit. Customers (end-users): If you received product from a distributor, please contact the distributor or your sales representative with any questions you may have. Distributors: If any of the affected kits identified in Appendix 1 were further distributed, please ensure all end-users are appropriately notified of this product correction and maintain records of effectiveness. "Complete the attached Recall Response Form and return as soon as possible. Report any quality problems or adverse events associated with the products listed in this notification to [email protected].
Recall details
- Recall number
- Z-0433-2025
- Status
- Open, Classified
- Initiated by the company
- Sep 20, 2024
- Posted by the FDA
- Nov 14, 2024
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 42 eaches
- Product code
- LRO
- Distribution
- US Nationwide distribution.
Product description
Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Model Number: SHAN431-07
Code information (models, lots, serial numbers)
GTIN: 10809160427224 Lot Number: 1612993
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Halyard SHAN431-07_0001Avid Medical, Inc. · General surgery tray1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 95515).
- Z-0383-2025 · Open, ClassifiedHalyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018
- Z-0384-2025 · Open, ClassifiedHalyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
- Z-0385-2025 · Open, ClassifiedHalyard D & C PACK-CKC - Medical convenience kits Model Number: BMGT003-02
- Z-0386-2025 · Open, ClassifiedHalyard ENT T AND A PACK - Medical convenience kits Model Number: EAMC106-02
- Z-0387-2025 · Open, ClassifiedHalyard OPEN HEART PACK MAIN - Medical convenience kits Model Number: ESJH003-02
- Z-0388-2025 · Open, ClassifiedHalyard AORTA PACK - Medical convenience kits Model Number: ESJH004-02
- Z-0389-2025 · Open, ClassifiedHalyard GENERAL SET UP PACK - Medical convenience kits Model Number: ESJH005-02
- Z-0390-2025 · Open, ClassifiedHalyard KIT, TOTAL KNEE - Medical convenience kits Model Number: ESJH012-07
- Z-0391-2025 · Open, ClassifiedHalyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
- Z-0392-2025 · Open, ClassifiedHalyard KIT, CARDIAC ROBOTIC - Medical convenience kits Model Number: ESJH017-03
- Z-0393-2025 · Open, ClassifiedHalyard ANTERIOR HIP PACK - Medical convenience kits Model Number: EUOR001-06
- Z-0394-2025 · Open, ClassifiedHalyard KIT, TOTAL KNEE - Medical convenience kits Model Number: EUOR002-05
- Z-0395-2025 · Open, ClassifiedHalyard KIT, TOTAL KNEE - Medical convenience kits Model Number: EUOR002-06
- Z-0396-2025 · Open, ClassifiedHalyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-02
- Z-0397-2025 · Open, ClassifiedHalyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-03
- Z-0398-2025 · Open, ClassifiedHalyard FOOT ANKLE PACK - Medical convenience kits Model Number: EUOR005-02
- Z-0399-2025 · Open, ClassifiedHalyard ABDOMINAL PROCEDURE - Medical convenience kits Model Number: GRAN015-06
- Z-0400-2025 · Open, ClassifiedHalyard BASIC PROCEDURE PACK - Medical convenience kits Model Number: GRAN019-06
- Z-0401-2025 · Open, ClassifiedHalyard TOTAL KNEE - Medical convenience kits Model Number: GRND008-09
- Z-0402-2025 · Open, ClassifiedHalyard CYSTO PDS - Medical convenience kits Model Number: GVVA002-05
- Z-0403-2025 · Open, ClassifiedHalyard MINOR PDS - Medical convenience kits Model Number: GVVA009-06
- Z-0404-2025 · Open, ClassifiedHalyard LAPAROSCOPY TRAY - Medical convenience kits Model Number: LANC006-25
- Z-0405-2025 · Open, ClassifiedHalyard GYN TRAY - Medical convenience kits Model Number: LANC014-19
- Z-0406-2025 · Open, ClassifiedHalyard C SECTION BUNDLE - Medical convenience kits Model Number: LANC015-34
- Z-0407-2025 · Open, ClassifiedHalyard VAG HYSTERECTOMY BUNDLE PK - Medical convenience kits Model Number: LANC022-29
- Z-0408-2025 · Open, ClassifiedHalyard POST PARTUM TUBAL LIGATION - Medical convenience kits Model Number: LANC026-19
- Z-0409-2025 · Open, ClassifiedHalyard TAH-BUNDLE - Medical convenience kits Model Number: LANC039-29
- Z-0410-2025 · Open, ClassifiedHalyard KNEE ARTHROSCOPY PACK - Medical convenience kits Model Number: MAMC204-16
- Z-0411-2025 · Open, ClassifiedHalyard LINE INSERTION PACK - Medical convenience kits Model Number: MAMC217-18
- Z-0412-2025 · Open, ClassifiedHalyard ANGIOGRAPHY PACK - Medical convenience kits Model Number: MAMC218-18
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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