FDADecember 23, 2015device
Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The sterile battery may contain particulates within the sterile package.
What to do
FDA enforcement status: Terminated
Brands named
pro dexpropro dex
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAPro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-112-112026-02-02
- FDAPro Numb Tattoo Numbing Spray, 5% Lidocaine, [1 FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing spray LLC, Melbourne, FL 32907, NDC 83389-111-112026-02-02
- CPSCScepter Fuel Containers Recalled Due to Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers; Imported by Pro Recycle2025-10-23
- CPSCMammut Sports Group Recalls Skywalker Pro Via Ferrata Sets Due to Risk of Serious Injury or Death from Fall Hazard2025-06-12
- CPSCSensio Recalls Steam Espresso Machines Due to Burn and Laceration Hazards2025-03-20
- FDADORO¿ Easy-Connect Navigation Adaptor; BRAINLAB (item No. 1204.002)2025-03-14
- CPSCBlack Diamond Equipment Recalls PIEPS Pro IPS Avalanche Transceivers Due to Risk of Loss of Emergency Communications2024-12-26
- CPSCPowerBlock Recalls Commercial Pro 100 Weight Sets Sold with 5 lb Grip Handles Due to Impact Injury Hazard2024-10-24
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