Z-1962-2025 Class II Ongoing

Recalled by Baxter Healthcare Corporation — Deerfield, IL

FDA device recall Z-1962-2025 was initiated by Baxter Healthcare Corporation on May 9, 2025 and is designated Class II. Reason for recall: The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and use… The recall status is ongoing. Affected quantity: 277 units.

Recall Details

Product Type
Devices
Report Date
June 18, 2025
Initiation Date
May 9, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
277 units

Product Description

2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600

Reason for Recall

The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and user burns.

Distribution Pattern

US Nationwide distribution.

Code Information

UDI/DI 00732094139488, Lot Number 25-043, Exp. August 2027