Recalls affecting Alabama

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-0682-2026

Lot/product code:

Lot: a)1505123, expires: 2027-04; b) 1505131, 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: Quantum 1450 0060650920009*7 K112815 D143578 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-0684-2026

Lot/product code:

Lot: a) 1505334, expires: 2027-04; b) 1505143, 1505151, expires: 2027-04

Recalling firm:

Bell Pharmaceuticals, Inc

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

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

Recall #:

D-0688-2026

Lot/product code:

Lot:1505141, 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: Quantum Outback 0060650920024*0 K112815 D143578 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

99286

Lot/product code:

Lot Code: Q6 Edge 3 Stretto 0060650920018*9 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 #:

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.

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

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-0674-2026

Lot/product code:

Lot, expiry: RAZM0425A Jun 30, 2027; RAZM0525A Jun 30, 2027; RAZM0725A Jun 30, 2027; RAZM0825A Jun 30, 2027; RAZM0925A Jul 31, 2027; RAZM1125A Jul 31, 2027; RAZM1225A Jul 31, 2027; RAZM1425A Jul 31, 2027; RAZM1525A Jul 31, 2027; RAZM1625A Aug 31, 2027; RAZM1725A Aug 31, 2027; RAZM2025A Sep 30, 2027

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

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.

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

Recall #:

99289

Lot/product code:

UDI-DI: 30695085407007; Lot Numbers: 4293568, 4293569, 4297510, 4297509, 4326087, 4337724, 4337725, 4346349

Recalling firm:

ICU Medical Inc.

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:

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

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:

S8698GX UDI-DI 20612479214716 Lot D5M3438FY

Recalling firm:

Covidien, LP

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

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

Recall #:

99359

Lot/product code:

Flow-i C20 6677200 / UDI-DI 07325710001349 Flow-i C30 6677300 / UDI-DI 07325710001363 Flow-i C40 6677400 / UDI-DI 07325710001318 Flow-i C20 6888520 / UDI-DI 07325710010617 Flow-i C30 6888530 / UDI-DI 07325710010624 Flow-i C40 6888540 / UDI-DI 07325710010631 Flow-c 6887700 / UDI-DI 07325710009765 Flow-e 6887900 / UDI-DI 07325710010457 Software versions 4.8, 4.10, and 4.11.

Recalling firm:

Maquet Critical Care AB

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: 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-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