Recalls affecting Oregon

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

Recall #:

D-0685-2026

Lot/product code:

Lot: a) 1505333, expires: 2027-04; b) 1505144, 1505302, expires: 2027-04.

Recalling firm:

Bell Pharmaceuticals, Inc

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

Recall #:

99286

Lot/product code:

Lot Code: 4Front 0060650920003*5 K143383 D246699 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

99304

Lot/product code:

Catalog Number: Astral 100 UDI-DI code: 00619498003259 Serial Numbers: Astral Ventilators-Serial number < 22241890149 PCBA Spare Parts via physical PCBA or Ventilator UI - Characters 2 8 < 2707658 PCBA Spare Parts in Box - Box serial number < 22241978070 Catalog Number: Astral 150 UDI-DI code: 00619498270033 Serial Numbers: Astral Ventilator-Serial numbers < 22241440282 PCBA Spare Parts via physical PCBA or Ventilator UI - Characters 2 8 < 2707658 PCBA Spare Parts in Box - Box serial number < 22241978070

Recalling firm:

ResMed Ltd.

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

Recall #:

99286

Lot/product code:

Lot Code: Quantum 4Front 2 0060650920019*6 K143383 D246699 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

D-0687-2026

Lot/product code:

Lot:1505344, exp 2027-04.

Recalling firm:

Bell Pharmaceuticals, Inc

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

Recall #:

99286

Lot/product code:

Lot Code: Q6 Edge 2.0 (ilevel) 0060650920004*2 K143383 D246699 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

D-0679-2026

Lot/product code:

Lot: a) 1504241, exp 2027-03; b) 1504291, 1504301, exp 2027-03.

Recalling firm:

Bell Pharmaceuticals, Inc

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

Recall #:

99286

Lot/product code:

Lot Code: Q6 Edge 4 0060650920028*8 K143383 D246699 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

99390

Lot/product code:

SP-623 UDI-DI 20884521037073 Lot D6A2963Y

Recalling firm:

Covidien, LP

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

Recall #:

99320

Lot/product code:

UDI-DI: 20763000135670, Lot Numbers: 0232601501 0232601510 0232601549 0232601550 0232602178 0232602290 0232602302 0232910952 0232910953 0232910954 0232910955 0233244075 0233244301 0233244531 0233286362 0233286374 0233286390 0233409034 0233416071 0233528731

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

99390

Lot/product code:

VLOCM0336 UDI-DI 20884521132501 Lot A5M0917VY VLOCM0436 UDI-DI 20884521827513 Lot A5M1035VY VLOCM0003 UDI-DI 10884521131606 Lot A5M1022VFY UDI-DI 20884521131603 Lots A5M1022VFY A5M1166VFY VLOCM0013 UDI-DI 10884521131644 Lot A5M1024VFY UDI-DI 20884521131641 Lots A5M1023VFY A5M1024VFY VLOCM0024 UDI-DI 10884521131699 Lot A5M0860VFY UDI-DI 20884521131696 Lot A5M0860VFY VLOCM0123 UDI-DI 20884521132235 Lot A5M1169VFY VLOCM0315 UDI-DI 20884521132464 Lot A6A1005VY VLOCM0603 UDI-DI 10884521132535 Lot A5M1246VY UDI-DI 20884521132532 Lot A5M1246VY VLOCM0604 UDI-DI 10884521132542 Lot A5M1062VY UDI-DI 20884521132549 Lots A5M1014VY A5M1062VY VLOCM1203 UDI-DI 10884521132757 Lot A6A1063VY UDI-DI 20884521132754 Lot A6A1063VY VLOCM2115 UDI-DI 20884521133003 Lot A5M1155VY

Recalling firm:

Covidien, LP

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

Recall #:

H-1150-2026

Lot/product code:

Lot # 0160933 Best by date of Jan 23, 2027

Recalling firm:

Lehi Valley Trading Company, Inc

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

Recall #:

99390

Lot/product code:

88861757-31 UDI-DI 10884521070912 Lot D6A3020FY UDI-DI 20884521070919 Lot D6A3020FY 88861799-31 UDI-DI 20884521071060 Lot D6A2861FY

Recalling firm:

Covidien, LP

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

Recall #:

D-0671-2026

Lot/product code:

Lot, expiry: RPTL0325A Dec 31, 2027; RPTL0425A Dec 31, 2027; RPTL0624B Nov 30,2027; RPTL0625A Mar 31, 2028

Recalling firm:

Reliance Life Sciences Private Limited

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

Recall #:

D-0673-2026

Lot/product code:

Lot, expiry: RBIH0125A Jan 31, 2028; RBIH0225A Feb 29, 2028; RBIH0325A Feb 29, 2028; RBIH0525A Mar 31, 2028

Recalling firm:

Reliance Life Sciences Private Limited

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

Recall #:

99320

Lot/product code:

UDI-DI: 20199150023251, Lot Numbers: 0232709184 0232745036 0232798416 0232862784 0232862787; UDI-DI: 00199150023257, Lot Numbers: 0232862787

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

99390

Lot/product code:

S8698GX UDI-DI 20612479214716 Lot D5M3438FY

Recalling firm:

Covidien, LP

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

Recall #:

99261

Lot/product code:

Part Number: 423742 UDI-DI code: 00815381020529 Pouch Lot: 3VLB25 Kit Lot: 1872125

Recalling firm:

BioFire Diagnostics, LLC

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

Recall #:

D-0732-2026

Lot/product code:

Lots: GY825029, GY825030, GY825031, GY825032, expires: 2028-OCT

Recalling firm:

JB Chemicals and Pharmaceuticals Ltd

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

Recall #:

99320

Lot/product code:

UDI-DI: 20199150023312, Lot Numbers: 0232657469 0232670800 0232744945 0232798410 0232862769 0232985251 0233116924 0233116931; UDI-DI: 00199150023318, Lot Numbers: 0232744945

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

D-0664-2026

Lot/product code:

Lot #: 10162261, 10162262, 10162279, 10162280, Exp. Date 07/21/2026; 10162314, 10162315, Exp. Date 07/22/2026; 10162465, 10162466, 10162491, 10162492, Exp. Date 07/26/2026; 10162542, 10162543, Exp. Date 07/27/2026; 10162559, 10162560, Exp. Date 07/28/2026; 10162623, 10162624, Exp. Date 07/29/2026; 10162693, 10162694, Exp. Date 07/30/2026; 10162735, 10162736, 10162753, 10162754, Exp. Date 07/31/2026; 10162772, 10162773, 10162791, 10162792, 10162810, 10162811, Exp. Date 08/02/2026; 10162820, Exp. Date 08/03/2026; 10162853, 10162854, Exp. Date 08/04/2026; 10163046, Exp. Date 08/09/2026; 10163156, 10163157, Exp. Date 08/10/2026.

Recalling firm:

QuVa Pharma, Inc.

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

Recall #:

D-0672-2026

Lot/product code:

Lot, expiry: RPTH0125A Jan 31, 2028; RPTH0225A Jan 31, 2028; RPTH0325A Jan 31, 2028; RPTH0725A Apr 30, 2028;

Recalling firm:

Reliance Life Sciences Private Limited

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

Recall #:

99320

Lot/product code:

UDI-DI: 20763000135700, Lot Numbers: 0232602300 0232602383 0232612916 0232680078 0232708967 0232709001 0232910880 0232910881 0232910882 0233077983 0233245850 0233245860 0233245980; UDI-DI: 00763000135706, Lot Numbers: 0232612916 0232709001

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

99320

Lot/product code:

UDI-DI: 20763000135632, Lot Numbers: 0232446429 0232446444 0232486752 0232601515 0232601516 0232601522 0232601586 0232601591 0232601593 0232602180 0232798265 0232798353 0232849583 0232894981 0232895082 0232902694 0232902697 0232902698 0232902700 0232902803 0232902805 0232902846 0232985469 0233009922 0233108251 0233116991 0233127352 0233334923 0233334966 0233426694 0233426695 0233528727; UDI-DI: 00763000135638, Lot Numbers: 0232446444 0232798353 0232895082 0232902697 0232902803 0232902846 0232985469 0233127352 0233334923

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

99320

Lot/product code:

UDI-DI: 00199150023288, Lot Numbers: 0233286436; UDI-DI: 20199150023282, Lot Numbers: 0232709428 0232744924 0232745061 0232745092 0232798556 0232862763 0232862778 0232862794 0232862798 0232903216 0232903291 0232903383 0232990983 0233286318 0233286414 0233286436 0233427120 0233528730 0233553623 0233556386 0233585113 0233585114 0232670802

Recalling firm:

Medtronic Perfusion Systems