FDA Device recall Z-1444-2015

Hardy Diagnostics cat no

• FDA Device
• Class II
• terminated
• Published 2015-04-22

On 2015-04-22 the FDA classified a Class II recall of Hardy Diagnostics cat no by Hardy Diagnostics, citing the firm is recalling HardyCHROM SS, Cat. no. G327 Lot no. 15037 due to a report of possible lack of color development in Shigella organisms in the referenced lot.

Read the official FDA Device notice

Product

Hardy Diagnostics cat no. G327 HardyCHROM SS Agar (HardyCHROM Salmonella Shigella) Cat no: G327 Container type: 15x100mm monoplate Packaged: 10 plates/sleeve Storage: 2 to 8 degrees C. on receipt in dark A selective chromogenic medium for the primary screening isolation, and differentiation of Salmonella & Shigella spp.

Reason

The firm is recalling HardyCHROM SS, Cat. no. G327 Lot no. 15037 due to a report of possible lack of color development in Shigella organisms in the referenced lot.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

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All Hardy Diagnostics recalls

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1444-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.