Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Welch Allyn PocketScope Replacement Batteries Recalled for Burn and Short Risk

Agency Publication Date: June 11, 2025
Share:
Sign in to monitor this recall

Summary

Baxter Healthcare Corporation is recalling 277 units of replacement rechargeable batteries used in Welch Allyn PocketScope handles. These batteries can cause a short circuit in the handle, leading to excessive heat and potentially burning the user. If you have these specific batteries, you should contact the manufacturer or your distributor immediately to arrange for a return or replacement.

Risk

The batteries may short circuit while inside the device handle, causing the equipment to overheat. This poses a significant risk of thermal burns to healthcare professionals or other users handling the device during medical examinations.

What You Should Do

  1. This recall involves 2.5 V replacement rechargeable batteries for Hillrom Welch Allyn PocketScope handles (Product Code 72600). Affected units are identified by UDI/DI 00732094139488 and Lot Number 25-043 with an expiration date of August 2027.
  2. Stop using the recalled battery and the PocketScope handle it is inserted into immediately.
  3. Contact Baxter Healthcare Corporation or your medical supply distributor to arrange for a return, replacement, or device correction.
  4. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Welch Allyn PocketScope Replacement Rechargeable Batteries (2.5 V)
Model / REF:
72600
Lot Numbers:
25-043 (Exp. August 2027)
UDI:
00732094139488

Recall #: Z-1962-2025; Quantity: 277 units.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96825
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: authorized medical distributors; hospital supply channels
Manufactured In: United States
Units Affected: 277 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.