OFFICIAL-SOURCE RECALL · AUSTRALIA
LABScreen Mixed Class I & II. An in vitro diagnostic medical device Recall: 21/09/2026 LABScreen Mixed Class
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
- LABScreen Mixed Class I & II. An in vitro diagnostic medical device (IVD).
- Manufacturer
- See official notice
- Lot number
- 026, specific
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
21/09/2026 LABScreen Mixed Class I & II. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Hazard
21/09/2026 LABScreen Mixed Class I & II. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Official recall notice
LABScreen Mixed Class I & II. An in vitro diagnostic medical device (IVD).
Agency: Therapeutic Goods Administration
Official publication date: September 21, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
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