OFFICIAL-SOURCE RECALL · AUSTRALIA
N Rheumatology Standard SL. An in vitro diagnostic medical device Recall: 16/09/2026 N Rheumatology Standard
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
- N Rheumatology Standard SL. An in vitro diagnostic medical device (IVD).
- Manufacturer
- See official notice
- Date code
- Dates
- Expiration date
- Dates
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
16/09/2026 N Rheumatology Standard SL. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Hazard
16/09/2026 N Rheumatology Standard SL. An in vitro diagnostic medical device (IVD). Medical Device Product Correction Class III Hospital
Official recall notice
N Rheumatology Standard SL. An in vitro diagnostic medical device (IVD).
Agency: Therapeutic Goods Administration
Official publication date: September 16, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
Keep an eye on the products at home.
Scan food and household product barcodes, save your items and get notified when a future recall may match.
