Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Diagnostic Use.
Reported: July 5, 2023 Initiated: May 31, 2023 #Z-2038-2023
Product Description
Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Diagnostic Use.
Reason for Recall
The test medium may not perform as intended.
Details
- Recalling Firm
- Remel, Inc
- Units Affected
- 1,296 packs
- Distribution
- Distribution was made nationwide, including Puerto Rico. There was no foreign or military distribution.
- Location
- Lenexa, KS
Frequently Asked Questions
What product was recalled? ▼
Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In Vitro Diagnostic Use.. Recalled by Remel, Inc. Units affected: 1,296 packs.
Why was this product recalled? ▼
The test medium may not perform as intended.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 5, 2023. Severity: Moderate. Recall number: Z-2038-2023.
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