PlainRecalls
FDA Devices Moderate Class II Terminated

Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US

Reported: July 15, 2020 Initiated: May 27, 2020 #Z-2488-2020

Product Description

Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US

Reason for Recall

Lack of assurance of sterility

Details

Units Affected
39800
Distribution
Nationwide
Location
Le Plessis Bouchard

Frequently Asked Questions

What product was recalled?
Prodimed Combicath catheters for mini bronchoalveolar lavage (BAL)-COMBICATH PE 85 cm x 4.0 mm 58124 40US. Recalled by Prodimed Plastimed Division. Units affected: 39800.
Why was this product recalled?
Lack of assurance of sterility
Which agency issued this recall?
This recall was issued by the FDA Devices on July 15, 2020. Severity: Moderate. Recall number: Z-2488-2020.