FDAClass IJanuary 1, 2020

Babi.Plus 12.5 cm H2O Pressure Relief Manifold recall

Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562

Why was Babi.Plus 12.5 cm H2O Pressure Relief Manifold recalled?

Reports of pressure relief manifold venting gas below the standard pressure.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI: 04710810093562 Lot: 180718, 181204, 190215, and 190610 (Reworked Product)

Product
Babi.Plus 12.5 cm H2O Pressure Relief Manifold, REF 1030, RX Only, UDI: 04710810093562
Recalling firm
Galemed Corporation
Quantity
2880
Distribution
US distribution to distributors in the states of: NC and NV.
Recall date
January 1, 2020
Classification
Class I
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls