Recalls affecting Minnesota

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

Recall #:

87654

Lot/product code:

all serial numbers

Recalling firm:

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

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

Recall #:

D-0381-2021

Lot/product code:

all lots

Recalling firm:

Hyobin LLC

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

Recall #:

D-0382-2021

Lot/product code:

all lots

Recalling firm:

Hyobin LLC

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

Recall #:

D-0383-2021

Lot/product code:

all lots

Recalling firm:

Hyobin LLC

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

Recall #:

87662

Lot/product code:

all codes

Recalling firm:

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

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

Recall #:

87662

Lot/product code:

all codes

Recalling firm:

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

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

Recall #:

87662

Lot/product code:

all codes

Recalling firm:

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

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

Recall #:

87705

Lot/product code:

UDI: 04015630939381

Recalling firm:

Roche Diagnostics Operations, Inc.

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

Recall #:

87705

Lot/product code:

UDI: 04015630939374

Recalling firm:

Roche Diagnostics Operations, Inc.

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

Recall #:

D-0642-2021

Lot/product code:

all lots

Recalling firm:

NSNY Distributor Inc

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

Recall #:

D-0641-2021

Lot/product code:

all lots

Recalling firm:

NSNY Distributor Inc

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

Recall #:

87682

Lot/product code:

Catalog Number: 7T Lot Numbers: U2101748 U2102001 U2102002 X2012711 X2103792

Recalling firm:

INNOVA MEDICAL GROUP, INC.

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

Recall #:

87682

Lot/product code:

Catalog Number: 25T REF: Bt1309 Lot Numbers: U2101750 U2101751 X2006004 X2008001 X2008010 X2009002 X2009004 X2009013 X2009016 X2010004 X2010010 X2011005 X2011006 X2011007 X2011008 X2011009 X2011012 X2011013 X2011015 X2011016 X2011017 X2011025 X2011051 X2011052 X2012001 X2012002 X2012004 X2012005 X2012008 X2101002 X2101004 X2101014 X2101031 X2101038

Recalling firm:

INNOVA MEDICAL GROUP, INC.

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

Recall #:

87682

Lot/product code:

Catalog Number: 3T Lot Numbers: U2102003 X2012310

Recalling firm:

INNOVA MEDICAL GROUP, INC.

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

Recall #:

D-0356-2021

Lot/product code:

Lot #13974 EXP 7/2021

Recalling firm:

Teligent Pharma, Inc.

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

Recall #:

87721

Lot/product code:

all batches/lots of the device manufactured between May 2018 through April 2021

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87721

Lot/product code:

all batches/lots of the device manufactured between May 2018 through April 2021

Recalling firm:

Boston Scientific Corporation

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

Recall #:

88146

Lot/product code:

Lot Number(s) 039406 Unique Device Identifier (UDI) 08717872016122

Recalling firm:

Dutch Ophthalmic USA, Inc.

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

Recall #:

87870

Lot/product code:

Part number: 910-414

Recalling firm:

Radiometer Medical ApS

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

Recall #:

87870

Lot/product code:

Model Number: ABL90 FLEX PLUS (393-092)   Serial Numbers: ABL90 FLEX PLUS analyzers serial numbers R0214 R0218, and R0223 onwards

Recalling firm:

Radiometer Medical ApS

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

Recall #:

87870

Lot/product code:

Model Number: ABL90 FLEX (393-090)  Serial Numbers: ABL90 FLEX analyzers with serial number R0996 R1000, and R1003 onwards

Recalling firm:

Radiometer Medical ApS

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

Recall #:

87709

Lot/product code:

All unexpired lots: C003726 C003737 C003739 C003752 C003767 C003778 C003782 C003791 C003814 C003818 C003831 C003845 C003846 C003874 C003875 C003898 C003899 C003921 C003942 C003954 C003970 C003988 C003989 C003999 C004000 C004011 C004012 C004031 C004032 C004033 C004048 C004049 C004084 C004085 C004086 C004097 C004098 C004099 C004120 C004132 C004143 C004150 C004159 C004175 C004176 C004196 C004205 C004213 C004218 C004223  GTIN: 08714729848103

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87766

Lot/product code:

Software version 9.3.1

Recalling firm:

Haag-Streit USA Inc

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

Recall #:

87709

Lot/product code:

All unexpired lots: C003699 C003715 C003735 C003750 C003775 C003804 C003813 C003842 C003853 C003887 C003905 C003936 C003950 C003960 C003966 C003986 C003997 C004028 C004041 C004078 C004091 C004107 C004117 C004128 C004136 C004160 C004186 C004206 C004221  GTIN 08714729848097

Recalling firm:

Boston Scientific Corporation

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

Recall #:

87802

Lot/product code:

Lot Number: 203373129 Exp. Date: June 30, 2022

Recalling firm:

Vygon U.S.A.