KLS Martin Battery Pack — Class II medical device recall Z-2098-2023
Ongoing recall by Pro-Dex Inc, reported 2023-07-12, distributed in FL. Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachm
| Recall number | Z-2098-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pro-Dex Inc, Irvine, CA, United States |
| Recall initiated | 2023-02-15 |
| Classified | 2023-07-05 |
| Reported by FDA | 2023-07-12 |
| Distributed | FL |
| Quantity | 2,000 |
| Reason classes | labeling, sterility |
| UPC / GTIN / UDI-DI | 00862377000140 |
| Lot numbers | K0M6U |
| Model numbers | 001, 040, KLS-BP-001/KLS-BP-040 |
| Expiration dates | 2024-08-31 |
Product
KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver
Reason for recall
Battery packs used in surgical procedures where a surgeon uses a powered screwdriver and a right-angle attachment have switched manufacturing and expiration dates on sterile pouch labels, so batteries will appear to be prematurely expired.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2098-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.