Device recall
Z-0501-2026: Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed…
FDA device recall · Class II · TECHNO-PATH MANUFACTURING LTD.
Key facts
| Recall number (Z-number) | Z-0501-2026 |
|---|---|
| Recall event | 97800 |
| Product | Multichem ID-B. Model/Catalog Number: SR103B Intended for use as an unassayed positive qualitative quality control serum to monitor the precision of laboratory testing procedures for the determination of anti-HIV-1 IgG, anti-HBc IgG, anti-HTLV-I IgG, anti-HCV IgG, HBs antigen and anti-Treponema… |
| Product code | OHQ |
| Recalling firm | TECHNO-PATH MANUFACTURING LTD. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3008156187 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database