PlainRecalls
FDA Devices Moderate Class II Terminated

B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01 4251890-01 4252535-01 4252586-01 4251644-01

Reported: December 9, 2020 Initiated: March 23, 2020 #Z-0509-2021

Product Description

B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01 4251890-01 4252535-01 4252586-01 4251644-01

Reason for Recall

Distribution of B.Braun Introcan Safety IV catheters without a 510(k) within the United States by JTG.

Details

Recalling Firm
Janus Trade Group
Units Affected
1365 cases (200 units/case)
Distribution
US distribution to distributors located in CA, FL, IL, KS, NJ, NY, and TN.
Location
Eatontown, NJ

Frequently Asked Questions

What product was recalled?
B. Braun Introcan Safety IV Catheters, Product codes REF 4252500-01 4252519-01 4252535-01 4252560-01 4252586-01 4251890-01 4252535-01 4252586-01 4251644-01. Recalled by Janus Trade Group. Units affected: 1365 cases (200 units/case).
Why was this product recalled?
Distribution of B.Braun Introcan Safety IV catheters without a 510(k) within the United States by JTG.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 9, 2020. Severity: Moderate. Recall number: Z-0509-2021.