Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported September 24, 2025
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiati…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
BigTree Sales Inc. recalled The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, t… - a moderate-severity action.
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, t… was recalled by BigTree Sales Inc. in September 24, 2025. Reason: The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Ris…. Check the official notice for the remedy. Verify recall #Z-2571-2025 with the FDA Devices before acting.
The recall
BigTree Sales Inc. issued this moderate-severity FDA Devices recall-The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Ris….
- Moderate
- severity level
- Class II
- classification
- September 24, 2025
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2571-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2571-2025) was formally reported on September 24, 2025, with the manufacturer initiating the action on August 29, 2025. It is classified under Moderate severity (Class II), with a current status of Ongoing. BigTree Sales Inc. is listed as the recalling firm, operating out of Arcadia, CA. Federal records list the affected scope as N/A.
The documented reason for this recall is: The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiatio… Distribution data in the federal record shows the product reached: U.S.A. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
N/A
Related Recalls
6
3 from same agency
Product description
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Reason for recall
The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2571-2025 |
| Date reported | September 24, 2025 |
| Date initiated | August 29, 2025 |
| Recalling firm | BigTree Sales Inc. |
| Firm location | Arcadia, CA |
| Affected scope | N/A |
| Distribution | U.S.A |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2571-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.. Recalled by BigTree Sales Inc.. Units affected: N/A.
Why was this product recalled? ▼
The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 24, 2025. Severity: Moderate. Recall number: Z-2571-2025.
Where was the recalled product distributed? ▼
Distribution: U.S.A.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2571-2025) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported September 24, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.