Oxoid™ Agglutinating Sera, Salmonella 9-0
Recall Summary OXOID™ Agglutinating Sera, Salmonella 9-0 is being recalled in New Zealand. The product is used in hospital, pharmacy, and laboratory settings to identify Salmonella bacteria. The manufacturer has determined the product must be destroyed.
- Recalling firm
- Thermo Fisher Scientific New Zealand Ltd
- Product
- OXOID™ Agglutinating Sera, Salmonella 9-0. [Device]. Affected: Lot - 6196409, 6233858, 6233859, 6260215, 6266130
- Reason
- An internal technical investigation has identified that certain lots of OXOID Agglutinating Sera, Salmonella 9-O, do not perform to Instructions for Use (IFU) criteria. Specifically, the affected lots show cross-reactivity with Salmonella 2-O within 60 seconds, which may lead to incorrect serogroup identification.
- Classification
- Class I
- Category
- medical device recall
- Country
- New Zealand
- Agency
- MEDSAFE
- Recall date
- 2026-04-01
- Status
- Ongoing
- Distribution
- New Zealand - Hospital/Pharmacy/Laboratory
Official recall notice from MEDSAFE
Recall details on Nibble Recalls: https://trynibble.app/recalls/8991caf1-5990-4818-a587-4978bf4a1799