FDA Enforcement Class II Ongoing

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.

Recall: Z-2038-2023 · Reported July 5, 2023

Enforcement

Recall Number
Z-2038-2023
Event ID
92444
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Remel, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 5, 2023
Initiation Date
May 31, 2023
Classification Date
June 29, 2023
Address
12076 Santa Fe Trail Dr, N/A, Lenexa, KS, 66215-3519, United States

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

The test medium may not perform as intended.

Code Info

REF R04033 lot numbers and expiration dates: Lot 619859 Exp. 2023-03-23, Lot 629086 Exp. 2023-03-31, Lot 629087 Exp. 2023-03-31, Lot 631001 Exp. 2023-04-11, Lot 634496 Exp. 2023-04-18, Lot 635369 Exp. 2023-04-19, Lot 645950 Exp. 2023-05-11, Lot 648004 Exp. 2023-05-18, and Lot 651372 Exp. 2023-05-23. UDI-DI #00848838004476. REF R01503 lot numbers and expiration dates: Lot 623548 Exp. 2023-03-28, Lot 631958 Exp. 2023-04-12, Lot 641527 Exp. 2023-05-02, Lot 644542 Exp. 2023-05-09, and Lot 648125 Exp. 2023-05-16. UDI-DI #00848838001932.

Distribution

Distribution was made nationwide, including Puerto Rico. There was no foreign or military distribution.

Quantity

1,296 packs