Recall Register

Food, drugs, devices › Firms

Pro-Dex Inc

FDA recalling firm · 5 enforcement events · 6 product records · 2015–2024 · CA

Pro-Dex Inc has 5 FDA enforcement events on this register (6 product records) between 2015 and 2024: 5 device; the busiest year was 2023 with 2.

0% of its events are Class I; the most common class is Class II (5). 3 events are listed as ongoing; the recalling firm's address is in CA.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

InitiatedProduct (first record)TypeClassRecordsStatus
23 Sep 2024KLS 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-2000DeviceClass II1Ongoing
15 Feb 2023KLS Martin Battery Pack, REF: KLS BP 001, and KLS BP 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriverDeviceClass II1Ongoing
14 Feb 2023KLS 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.DeviceClass II1Ongoing
25 Sep 2018PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery Pack, 40 Pouches - PDBP-040-2 Product Usage: -The PDBP-001 Battery is a single use (non-rechargeable) sterile lithium ion battery accessory that powers the PDSD Surgical driver. There is only one PDSD…DeviceClass II1Terminated
23 Dec 2015Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).DeviceClass II2Terminated

By type and class

Device5
Class II5

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

15
16
17
18
19
20
21
22
23
24
25
26
Enforcement events for Pro-Dex Inc by year initiated.

Questions and answers

How many FDA recalls has Pro-Dex Inc had?

5 enforcement events (6 product records) on this register, 2015–2024: 5 device.

Are any Pro-Dex Inc recalls ongoing?

3 events are listed as ongoing in the current openFDA export.

What class are Pro-Dex Inc recalls?

5 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.