Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1444-2015 — 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 differentiat

U.S. FDA — Device Enforcement · United States · 2015-03-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1444-2015
Date of alert: 2015-03-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hardy Diagnostics
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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