Recalls affecting Wyoming

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

Recall #:

88199

Lot/product code:

Serial Numbers:  1911040132 1911040133   UDI: 07613327282665

Recalling firm:

Stryker Medical Division of Stryker Corporation

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

Recall #:

87942

Lot/product code:

Lot # 115T1035

Recalling firm:

Encore Medical, LP

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:  031528600216109 051428600212599 081328600206460 UDI: 07613327298512

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:  2017000300284  UDI: 07613327322569

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:  F09519 F50699  UDI:07613327169348

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#) 07613327278149 07613327278149 07613327278194

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:  N/A UDI: 07613327282511

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 #:

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:

Serial Numbers: 1202033898 1206032470 1406034563 1607037109   UDI (DI#): 07613327282566

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-0778-2021

Lot/product code:

Lot No: GV4420205 Best By, 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#): 07613327278187

Recalling firm:

Stryker Medical Division of Stryker Corporation

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

Recall #:

87942

Lot/product code:

Lot # 155T1035

Recalling firm:

Encore Medical, LP

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

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

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:  R52495 R53376 R55047 R56034 M14805 M14885 M14886 M14931 M14936 M14938 M14939 M50074 M50425 M50951 M50956 M54387 R63407 R54523 R54610 R54696 R54698 R60775 R32649 R25384 R35631 R35734 R58735 M15330 R58474  UDI:   07613327169355 07613327169386

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 #:

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)