Recall · FDA

Baxter Healthcare Corporation

Baxter Healthcare Corporation issued a Class II FDA recall (Z-1144-2022) initiated 2022-04-21: Effluent Sample Bag

CompanyBaxter Healthcare Corporation
Recall numberZ-1144-2022
ClassificationClass II
StatusTerminated
CategoryDevices
Initiated2022-04-21
ProductEffluent Sample Bag
ReasonCertain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

FAQ

What did Baxter Healthcare Corporation recall?

Effluent Sample Bag

Why was Baxter Healthcare Corporation's product recalled?

Certain Peritoneal Dialysis product codes do not have FDA regulatory clearance and were distributed within the United States in error.

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