--- title: "Pro-Dex Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Pro-Dex Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/pro-dex-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Pro-Dex Inc recall records **3** reported ongoing 3 records in this archive. Latest source date Sep 23, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Sep 23, 2024 FDA device enforcement ### [KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000](https://isitonrecall.com/recall/fda-device-z-0280-2025-kls-martin-battery-pack-ref-kls-bp2-001-and-kls-bp2-040-bulk-case-of-40-used-in-conjunction-with-the/) The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package. Class II Reported ongoing Distribution: US distribution to FL only. [Official source for KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0280-2025%22) Feb 15, 2023 FDA device enforcement ### [KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver](https://isitonrecall.com/recall/fda-device-z-2098-2023-kls-martin-battery-pack-ref-kls-bp-001-and-kls-bp-040-bulk-case-of-40-used-in-conjunction-with-the-k/) 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. Class II Reported ongoing Distribution: US: FL [Official source for KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction w...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2098-2023%22) Feb 14, 2023 FDA device enforcement ### [KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to connect the KLS driver (e.g. drill) to a driver bit that fits into the adapter.](https://isitonrecall.com/recall/fda-device-z-1391-2023-kls-martin-group-kls-e-coupling-adapter-ref-pdec-1000-2-e-coupling-adapter-assembly-used-to-connect/) Incorrect Unique Device Identifier/GTIN code was used on product. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of FL. [Official source for KLS martin Group KLS E-COUPLING ADAPTER REF PDEC-1000-2 E-Coupling Adapter Assembly used to conne...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1391-2023%22) ## Reasons in these listed records - The packaging of a sterile battery, intended to power a surgical screwdriver, may contain Tyvek shavings inside the sterile package. - 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. - Incorrect Unique Device Identifier/GTIN code was used on product. These examples come from this result page and are not a ranking of every recall reason. ## Checking Pro-Dex Inc ### Is there a recall on pro-dex inc right now? This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Pro-Dex Inc](https://isitonrecall.com/check/?q=Pro-Dex%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)