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Use caution Medical device recall · FDA · Published May 9, 2025

Baxter Healthcare: 2.5V PocketScope Batteries Risk Burns from Short Circuit

Baxter Healthcare recalls 2.5V rechargeable batteries for Welch Allyn PocketScope handles that may cause short circuits and burns. Product code 72600, lot 25-043, expires August 2027.

🇺🇸 FDA recall #Z-1962-2025Medical deviceBaxter Healthcare ›
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Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
✎ GovInfoNow plain-language explainer

Baxter Healthcare is recalling 2.5V replacement rechargeable batteries for Welch Allyn PocketScope handles. These batteries can cause short circuits that lead to heat exposure and burns if used improperly. Read more at govinfonow.com/recall/52315-baxter-healthcare-2-5v-pocketscope-batteries-risk-burns-from-short.

Source Summary by GovInfoNow · govinfonow.com/recall/52315-baxter-healthcare-2-5v-pocketscope-batteries-risk-burns-from-short · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1962-2025

Cite this page

“Baxter Healthcare: 2.5V PocketScope Batteries Risk Burns from Short Circuit.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52315-baxter-healthcare-2-5v-pocketscope-batteries-risk-burns-from-short. Based on FDA recall #Z-1962-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1962-2025%22&limit=1).

Baxter Healthcare Corporation voluntarily recalled 277 units of 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles due to a short circuit hazard that can cause excessive heat and user burns, the FDA announced on May 9, 2025.

How to tell if you have it

  • Brand: Baxter Healthcare
  • Product: 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles
  • Product Code: 72600
  • UDI/DI: 00732094139488
  • Lot Number: 25-043
  • Expiration: August 2027

The hazard

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.

Context

GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls of similar products include Medline Semi Electric Lightweight Bed Recall (November 26, 2025), Medline beds recall (November 26, 2025), and Medline Full Electric Low Bed Recall (November 26, 2025).

How to tell if you have this one

Check for Product Code 72600 on the battery packaging. The lot number is 25-043 and the expiration date is August 2027.

  • Brand
    Baxter Healthcare
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Battery Packaging

    Look for Product Code 72600, Lot Number 25-043, and Expiration Date August 2027 on the battery packaging.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: May 9, 202512. FDA classified it Class II: Jun 11, 202523. Published in FDA’s Enforcement Report: Jun 18, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Do I need to stop using these batteries immediately?

The recall does not require immediate stop use; however, you should check if your batteries match the recalled specifications.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1962-2025 (May 9, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1962-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA