Recalls affecting Idaho

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

Recall #:

89190

Lot/product code:

Lots #: 0552101A596, 0552101A602 GTIN#: 07613327461503

Recalling firm:

Howmedica Osteonics Corp.

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

Recall #:

89375

Lot/product code:

S/N: OUS 109

Recalling firm:

Philips North America Llc

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

Recall #:

89173

Lot/product code:

All units are impacted

Recalling firm:

Philips North America Llc

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

Recall #:

89163

Lot/product code:

All units are impacted

Recalling firm:

Philips North America Llc

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

Recall #:

89163

Lot/product code:

All units are impacted

Recalling firm:

Philips North America Llc

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

Recall #:

89163

Lot/product code:

All units are impacted

Recalling firm:

Philips North America Llc

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

Recall #:

89163

Lot/product code:

All units are impacted

Recalling firm:

Philips North America Llc

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

Recall #:

D-0295-2022

Lot/product code:

Lot #: 16345, Exp. Date 01/2024

Recalling firm:

Teligent Pharma, Inc.

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

Recall #:

D-0296-2022

Lot/product code:

Lot #: 15594, Exp Date 05/2023

Recalling firm:

Teligent Pharma, Inc.

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

Recall #:

89437

Lot/product code:

Wireless Foot switch 3P : 459801238191  Wireless Foot switch 3P: 459801238231

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

89437

Lot/product code:

Wireless Foot switch 3P : 459801238191  Wireless Foot switch 3P: 459801238231

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

89437

Lot/product code:

Wireless Foot switch 3P : 459801238191  Wireless Foot switch 3P: 459801238231

Recalling firm:

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

Recall #:

89086

Lot/product code:

Lot numbers 02010697711582590 and 02010697711582591, GTIN 00840420108340.

Recalling firm:

Wright Medical Technology, Inc.

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

Recall #:

89089

Lot/product code:

Lot #1642103

Recalling firm:

Wright Medical Technology Inc

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

Recall #:

89089

Lot/product code:

Lot #1643355

Recalling firm:

Wright Medical Technology Inc

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

Recall #:

89167

Lot/product code:

Alinity m System, Model 08N53-002, all serial numbers

Recalling firm:

Abbott Molecular, Inc.

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

Recall #:

89168

Lot/product code:

Alinity m System, Model 08N53-002, all serial numbers

Recalling firm:

Abbott Molecular, Inc.

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

Recall #:

89166

Lot/product code:

Model 08N53-002, all serial numbers

Recalling firm:

Abbott Molecular, Inc.

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

Recall #:

89369

Lot/product code:

Serial Numbers: XCONUS0013 XCONUS0079 XCONUS0105 XCONUS0036 XCONUS0044 XCONUS0004 XCONUS0014 XCONUS0080 XCONUS0109 XCONUS0021 XCONUS0066 XCONUS0027 XCONUS0017 XCONUS0084 XCONUS0061 XCONUS0043 XCONUS0089 XCONUS0059 XCONUS0019 XCONUS0085 XCONUS0051 XCONUS0047 XCONUS0005 XCONUS0042 XCONUS0020 XCONUS0086 XCONUS0110 XCONUS0055 XCONUS0010 XCONUS0083 XCONUS0022 XCONUS0087 XCONUS0111 XCONUS0064 XCONUS0053 XCONUS0121 XCONUS0023 XCONUS0088 XCONUS0112 XCONUS0002 XCONUS0056 XCONUS0018 XCONUS0024 XCONUS0090 XCONUS0113 XCONUS0003 XCONUS0006 XCONUS0054 XCONUS0030 XCONUS0091 XCONUS0115 XCONUS0007 XCONUS0052 XCONUS0081 XCONUS0032 XCONUS0094 XCONUS0116 XCONUS0012 XCONUS0073 XCONUS0008 XCONUS0039 XCONUS0095 XCONUS0118 XCONUS0070 XCONUS0009 XCONUS0040 XCONUS0096 XCONUS0025 XCONUS0072 XCONUS0001 XCONUS0049 XCONUS0092 XCONUS0026 XCONUS0075 XCONUS0011 XCONUS0058 XCONUS0093 XCONUS0028 XCONUS0082 XCONUS0045 XCONUS0067 XCONUS0097 XCONUS0122 XCONUS0048 XCONUS0065 XCONUS0068 XCONUS0098 XCONUS0123 XCONUS0063 XCONUS0029 XCONUS0069 XCONUS0099 XCONUS0124 XCONUS0031 XCONUS0035 XCONUS0074 XCONUS0100 XCONUS0034 XCONUS0071 XCONUS0046 XCONUS0076 XCONUS0102 XCONUS0038 XCONUS0060 XCONUS0050 XCONUS0077 XCONUS0103 XCONUS0041 XCONUS0062 XCONUS0015 XCONUS0078 XCONUS0104 XCONUS0033 XCONUS0037 XCONUS0016 UDI: Prefix: 4057224 (+ serial number)

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

89125

Lot/product code:

UDI: 07325710008430 Serial Nos. 15580 15890 15924 16284 16637 16837 16970 15582 15891 15925 16285 16638 16840 16971 15721 15894 16268 16345 16639 16842 15722 15914 16269 16352 16640 16843 15725 15917 16270 16354 16690 16844 15726 15919 16271 16632 16828 16961 15728 15920 16272 16633 16832 16964 15729 15921 16273 16634 16833 16965 15731 15922 16276 16635 16834 16966 15732 15923 16283 16636 16836 16968

Recalling firm:

Getinge Usa Sales Inc

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

Recall #:

89383

Lot/product code:

Dunnage case consists of a random unknown lot, which may have been shipped in place of Kit lot K341

Recalling firm:

Mallinckrodt Pharmaceuticals Ireland Ltd

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

Recall #:

89362

Lot/product code:

UDI 10758750006786  Lot 1039734

Recalling firm:

Ortho-Clinical Diagnostics, Inc.

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

Recall #:

89309

Lot/product code:

UDI (01)07290017 08201 1 (10) YYMMDDXX (11)YYMMDD (17)YYMMDD, Lot Numbers: 21072510 and 21072512.

Recalling firm:

FEMSelect Ltd

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

Recall #:

89443

Lot/product code:

Lot Numbers: 50971615, 50971617 & 50967788

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

89235

Lot/product code:

Item Numbers: 1) CUR959/CUR959H (Lots 69718070004, 69718090003, 69718100001, 69718100004, 69718110003, 69719010001, 69719030001, 69719030004, 69719040002, 69719070005, 69719080002, 69719080006, 69719090001, 69719090004, 69719100001, 69719100004, 69719110001, 69719110003, 69719110004, 69719120001, 69719120005, 69719120002, 69719120006, 69720010001, 69720020002, 69720040001, 69720050001, 69720060001, 69720060002, 69720080002, 69720090001, 69720090002, 69720100001, 69720100002, 69720110002, 69720120001, 69720120002, 69721010001, 69721020001, 69721030001, 69721030002, 69721050001, 69721050002, 69721050003, 69721060001, 69721060002, 69721070001, 69721080002, 69721090001) 2) TGT0114V1 (Lots 69718070004, 69718080002, 69718090002 , 69718100004, 69718110003, 69719010001, 69719030004, 69719040002, 69719050002, 69719050004, 69719060001, 69719060003, 69719070001, 69719070005, 69719080002, 69719080006, 69719090004, 69719100001, 69719100004, 69719100005, 69719110001, 69719110002, 69719110004, 69719110003, 69719120005, 69719120002, 69719120007, 69719120006, 69720010001, 69720070001, 69720070002, 69720080001, 69720080002, 69720100003)

Recalling firm:

MEDLINE INDUSTRIES, LP - Northfield