Recalls affecting Kansas

FDA has not published a risk classification for this recall yet.

Recall #:

88622

Lot/product code:

All Serial numbers

Recalling firm:

CardioQuip, LLC

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0778-2021

Lot/product code:

Lot No: GV4420205 Best By, 5/21/2022

Recalling firm:

Global Sanitizers LLC

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0779-2021

Lot/product code:

Lot No: E372020, "Best Buy": 5/21/2022;

Recalling firm:

Global Sanitizers LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  031528600216109 051428600212599 081328600206460 UDI: 07613327298512

Recalling firm:

Stryker Medical Division of Stryker Corporation

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0782-2021

Lot/product code:

Lot No: E212020, "Best Buy": 5/21/2022

Recalling firm:

Global Sanitizers LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  120916611 121016000 130115957 130815166 UDI: 07613327278309

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  N/A UDI: 07613327282511

Recalling firm:

Stryker Medical Division of Stryker Corporation

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0781-2021

Lot/product code:

Lot No: E082020, "Best Buy": 5/21/2022

Recalling firm:

Global Sanitizers LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

UDI (DI#) 07613327278149 07613327278149 07613327278194

Recalling firm:

Stryker Medical Division of Stryker Corporation

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:

D-0783-2021

Lot/product code:

Lot No: E332020, E212020 "Best Buy": 5/21/2022

Recalling firm:

Global Sanitizers LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  U54274 U71491 UDI:07613327169294

Recalling firm:

Stryker Medical Division of Stryker Corporation

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:

D-0780-2021

Lot/product code:

Lot No: E082020, "Best Buy": 5/21/2022

Recalling firm:

Global Sanitizers LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  111427102713678 UDI:N/A

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  20170928500311838 UDI: 07613327277852 07613327277937

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  219009000417  UDI: 07613327278453

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88622

Lot/product code:

All Serial numbers

Recalling firm:

CardioQuip, LLC

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

UDI (DI#): 07613327278330

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88199

Lot/product code:

Serial Numbers:  FL23J50576 FL23J50577 FL23J60424 FL23J60627 J32346 J32347 J32348 J32350 J29770  UDI: N/A

Recalling firm:

Stryker Medical Division of Stryker Corporation

FDA has not published a risk classification for this recall yet.

Recall #:

88056

Lot/product code:

Effected SN Range: CM00902 - CM02065  Note: xxxx in serial number is any number.   UDI: 00630414002163

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

88056

Lot/product code:

Effected Serial Range: IM00873 IM01452 and IRM00256xxxx IRM01169xxxx Note: xxxx in serial number is any number.   UDI: 00630414007960

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

88056

Lot/product code:

Effected serial range: IH00876 IH01451 and IRH00258xxxx IRH01169xxxx  Note: xxxx in serial number is any number.     UDI: 00630414002026

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

FDA has not published a risk classification for this recall yet.

Recall #:

88089

Lot/product code:

Model Number: LNQ22

Recalling firm:

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA has not published a risk classification for this recall yet.

Recall #:

90490

Lot/product code:

Model 712032 Serial Numbers -  10001088  10001097  10001104  10001112  19000317 10001095  10001102  10001105

Recalling firm:

Philips Medical Systems DMC GmbH

FDA has not published a risk classification for this recall yet.

Recall #:

88120

Lot/product code:

Lot Numbers: 16F20C0035 16F20F0124

Recalling firm:

Arrow International Inc

FDA has not published a risk classification for this recall yet.

Recall #:

88120

Lot/product code:

Lot Numbers: 16F19J0109

Recalling firm:

Arrow International Inc