BIOPHEN UFH Control Plasma
Reported: September 21, 2022 Initiated: June 28, 2022 #Z-1743-2022
Product Description
BIOPHEN UFH Control Plasma
Reason for Recall
Incorrect product labeling was included in the package.
Details
- Recalling Firm
- Aniara Diagnostica LLC
- Units Affected
- 13 units (1 unit is 1 box)
- Distribution
- Distribution in US - IL and MI
- Location
- West Chester, OH
Frequently Asked Questions
What product was recalled? ▼
BIOPHEN UFH Control Plasma. Recalled by Aniara Diagnostica LLC. Units affected: 13 units (1 unit is 1 box).
Why was this product recalled? ▼
Incorrect product labeling was included in the package.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 21, 2022. Severity: Low. Recall number: Z-1743-2022.
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