Key Sun Kids Cough Homeopathic Product Multipack Lozenges and Kids Cold Homeopathic Product Raspberry Lozenges
AustraliaKey Sun Kids Cough Homeopathic Product Multipack Lozenges and Kids Cold Homeopathic Product Raspberry Lozenges
Recalling Firm: TGA
Reason for Recall / Hazard
Key Sun Laboratories Pty Ltd is recalling four batches of lozenges due to the risk of a small metal wire being present in the lozenge....
Product Description & Identification
Key Sun Laboratories Pty Ltd is recalling four batches of lozenges due to the risk of a small metal wire being present in the lozenge.
Affected Products
Key Sun Kids Cough Homeopathic Product Multipack Lozenges and Kids Cold Homeopathic Product Raspberry Lozenges
Additional Source Details
| Field | Value |
|---|---|
| Guid › #text | https://www.tga.gov.au/node/566787 |
| Guid › @ is Perma Link | true |
| Link | https://www.tga.gov.au/safety/recalls-and-other-market-actions/market-actions/key-sun-kids-cough-homeopathic-product-multipack-lozenges-and-kids-cold-homeopathic-product-raspberry-lozenges |
| Pub Date | Fri, 10 Jul 2026 00:00:00 +1000 |
| Extracted category | devices |
Overview
- Recalling FirmTGA
- Risk LevelMedical Device Correction
- DistributionAustralia
📢 Share Warning
Alert family and friends to keep them safe. Copy this quick alert message:
🚨 SAFETY ALERT: TGA - Key Sun Kids Cough Homeopathic Product Multipack Lozenges and Kids Cold Homeopathic Product Raspberry Lozenges Check if your household is affected: https://therecallfile.com/recalls/key-sun-kids-cough-homeopathic-product-multipack-lozenges-and-kids-col/AU-TGA-566787
Join Alertlist
Get instant email updates whenever critical safety recalls like this are published.
Related Recalls
UKField Safety Notices: 13 to 17 July 2026
Field Safety Notices: 13 to 17 July 2026
List of Field Safety Notices from 13 to 17 July 2026....
FDA DevicesAquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R
Surgical dressing manufactured out of specification (greater thickness).
FDA DevicesGSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.
Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.