OFFICIAL-SOURCE RECALL · AUSTRALIA
ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD) Recall: 22/09/2026 ID-DiaCell I-II-III
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD).
- Manufacturer
- See official notice
- Lot number
- 133842941, 45184, from
- Batch number
- 45184, 133842941, from
- Date code
- Date
- Expiration date
- Date
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
22/09/2026 ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Hazard
22/09/2026 ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD). Medical Device Recall Class II Hospital
Official recall notice
ID-DiaCell I-II-III. An in vitro diagnostic medical device (IVD).
Agency: Therapeutic Goods Administration
Official publication date: September 22, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
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