Churchill Medical Systems, Inc. Recalls

Recall history in this database

Classification mix: Class II: 9.

Medical DeviceApr 29, 2015

Churchill Medical Systems 4" Trifurcated set with Bionectors and check valves, Product Code recall — FDA Z-1477-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 4" Microbore Trifurcated Ext set, Product Code: BN-308 Accessory recall — FDA Z-1470-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 6" Trifurcated set with Bionectors, Product Code: BN-944 Accessory recall — FDA Z-1478-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 recall — FDA Z-1474-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 4" Microbore Double Lumen Set with Bionector, Product Code: BN-208 recall — FDA Z-1469-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 7" High Pressure Set with Bionector, Product Code: CMS-808 and recall — FDA Z-1473-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 8" Standard Bore Ext Set, Product Code: BN-481 Accessory device recall — FDA Z-1472-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems Bifurcated set with check vales and Bionectors, Product Code recall — FDA Z-1476-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Medical DeviceApr 29, 2015

Churchill Medical Systems 7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 recall — FDA Z-1475-2015

Potential for leaking caused by insufficient bond between needleless device and female luer.

Class IIFDA: TerminatedChurchill Medical Systems, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Churchill Medical Systems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.