DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
Reported: May 10, 2023 Initiated: March 20, 2023 #Z-1506-2023
Product Description
DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
Reason for Recall
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
Details
- Recalling Firm
- DermLite LLC
- Units Affected
- 32 units
- Distribution
- Worldwide - US Nationwide distribution in the states of CA, AZ, TX, FL, NE, IA, MO, CO and the countries of Saudi Arabia, Australia, Spain.
- Location
- San Juan Capistrano, CA
Frequently Asked Questions
What product was recalled? ▼
DERMLITE DL4W, REF: DL4W, Rx Only MD, CE. Recalled by DermLite LLC. Units affected: 32 units.
Why was this product recalled? ▼
Incorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 10, 2023. Severity: Moderate. Recall number: Z-1506-2023.
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