Official recall record
Multichem S Plus, Part Codes: a) 08P88-10, b) 08P88-11, c) 08P88-12
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-08-25
- Country of alert
- Ireland
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 05391523440776
- Brand on record
- TECHNO-PATH MANUFACTURING LTD.
What the authority reported
Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem IA Plus and Multichem P Controls. Some customers have experienced broken vials when receiving or thawing Technopath Multichem IA Plus and Multichem S Plus Controls. Breakages have been observed upon delivery, while thawing or while opening the vial. The breakages can result in the bottom of the vial breaking off, breakage in the neck thread area or cracking on the sides of the vial. This may expose the user to biohazardous material if cut and may cause a delay in patient results.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2026-08-14 · US FDA — Medical Devices
Techno-Path Multichem AE Unassayed Level 2 REF: AE622X - 2026-08-14 · US FDA — Medical Devices
Techno-Path Multichem AE Unassayed Level 1 REF:AE621X - 2026-08-14 · US FDA — Medical Devices
Techno-Path Multichem AE Unassayed Level 3, REF:AE623X
All 5 official recall notices naming TECHNO-PATH MANUFACTURING LTD. on this site →