Home › U.S. Biotek Laboratories LLC › US Biotek Laboratories
US Biotek Laboratories
U.S. Biotek Laboratories LLC · Model 1.0 · UDI-DI 00860010959268
PQD
Prescription
0
510(k) clearances
19
Adverse events
1
Recalls
55
Facilities
Description
Single-use convenient serum collection kit includes collection tube(s), and return packing for mailing to testing laboratory.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-03-16 | LetsGetChecked Inc. | Users received sample collection kits that were assigned to another user. Incorrect shipping labels were applied to the collection kits. As a result, a number of users received sa |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.