Well at Walgreens 930448Recalls & reported problems
Walgreen CO. · Freeze Wart Remover · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00311917182216), received between Mar 31, 2020 and Mar 31, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Human-Device Interface Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Human-Device Interface Problem1
Patient problems
- Patient Problem/Medical Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2020Human-Device Interface Problem; Human-Device Interface Problem
ON 3/27/2020 AT 8:29 P.M. AN E-MAIL WAS RECEIVED BY WALGREEN'S CONSUMER RELATIONS TO ORASURE TECHNOLOGIES INC. TECHNICAL SERVICES IN REGARDS TO A CONSUMER ADVERSE EVENT. THE CONSUMER STATED THAT THEY HAD AN ADVERSE REACTION TO THE WALGREENS FREEZE WART REMOVER PRODUCT. THE PRODUCT "CAUSED A HOLE IN MY NOSE" AS THE CONSUMER STATED. THE CONSUMER ALSO STATED THAT IS HAS BECOME A NAGGING ISSUE AND THEY COULD NOT GET IT FIXED WITHOUT PLASTIC SURGERY. THE CONSUMER FELT LIKE THERE SHOULD HAVE BEEN SOME KIND OR WARNING OR NOTICE. A PHONE CONVERSATION WAS HELD WITH THE CONSUMER AND ORASURE TECHNOLOGIES INC.'S TECHNICAL SERVICES ON 3/30/2020. THE CONSUMER STATED THAT THERE WAS NO PRODUCT INSTRUCTIONS INLCLUDED WITH THEIR WALGREENS FREEZE KIT SO THEY USED WHAT WAS REFERENCED ON THE BOX INSTEAD. PICTURES OF THE SKIN DAMAGE WAS PROVIDED TO ORASURE TECHNOLOGIES INC. VIA E-MAIL FROM THE CONSUMER.
Patient problems: Patient Problem/Medical Problem
MAUDE report 9902979 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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