Recalls affecting Alabama

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

Recall #:

99349

Lot/product code:

UDI: 15099590799250/ V5.03 Panel Update 11

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

99341

Lot/product code:

UDI-DI 04050147013797/ Serial Numbers: All serial numbers up to 11608268 Software Version: 1.0.3

Recalling firm:

Erbe USA Inc

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

Recall #:

99379

Lot/product code:

UDI-DI 00842768001406 Lot U1

Recalling firm:

Siemens Healthcare Diagnostics, Inc.

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

Recall #:

99349

Lot/product code:

UDI: 15099590799243/ V5.03 Panel Update 11

Recalling firm:

Beckman Coulter Inc.

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

Recall #:

D-0683-2026

Lot/product code:

Lot: 1505124, 1505311, 1505332, 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-0680-2026

Lot/product code:

Lot: a) 1505121, 1505342, exp 2027-04; b) 1505381, 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 4Front 2 0060650920019*6 K143383 D246699 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: Quantum Outback 0060650920024*0 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-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 #:

98840

Lot/product code:

SureStep Intermittent Catheter Tray INTP16 / 00801741183300¿ 10801741183307 Lot Numbers: NGKT3672 NGKU1467 NGKU3559 INTS14 / 00801741183218 10801741183215 Lot Numbers: NGKT2630 NGKT2687 NGKT3636 NGKT3673 NGKU0119 NGKU0134 NGKU1412 NGKU1439 NGKU1494 NGKU2451 NGKU2487 NGKU2510 INTS14C / 00801741183232 10801741183239 Lot Numbers: NGKT2660 NGKU0149 NGKU1468 INTS16 / 00801741183225 10801741183222 Lot Numbers: NGKT2688 NGKT3587 NGKU0135 NGKU2423 INTS16C / 00801741183249 10801741183246 Lot Numbers: NGKT2631 NGKU0120 NGKU1413 PEDINTS06 / 00801741183263¿ 10801741183260 Lot Number: NGKU2452 PEDINTS08 / 00801741183270 10801741183277 Lot Numbers: NGKT3637 NGKU0166 NGKU1495 PEDINTS10 / 00801741183287¿ 10801741183284 Lot Number: NGKT3674 Pre-amendment INTL14 / 00801741183164 10801741183161 Lot Numbers: NGKT3670 NGKU0132 NGKU1491 INTL15 / 00801741183171 10801741183178 Lot Numbers: NGKT2658 NGKT3584 NGKT3609 NGKU0116 NGKU0118 NGKU0133 NGKU0147 NGKU0163 NGKU1411 NGKU1436 NGKU1437 NGKU1465 NGKU1466 NGKU1492 NGKU2421 NGKU2449 NGKU2450 NGKU2485 NGKU2486 NGKU2508 NGKU2509 NGKU4598 NGKU4601 INTL16 / 00801741183188 10801741183185 Lot Number: NGKU3558 INTP14 / 00801741183294 10801741183291 Lot Numbers: NGKT2659 NGKT3585 NGKT3610 NGKT3635 NGKU0148 NGKU1438 NGKU3567

Recalling firm:

C.R. Bard Inc

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

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

Recall #:

98840

Lot/product code:

SureStep" Foley Tray System Add-A-Foley Catheter A153200 / 00801741121067¿ 10801741121064 Lot Number: NGKS2397 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter A304400A / 00801741073847¿ 10801741073844 Lot Numbers: NGKU1023 NGKU3043 SureStep" Foley Tray System Add-A-Foley Catheter A399400 / 00801741100369¿ 10801741100366 Lot Number: NGKU2042 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter A399400A / 00801741073915¿ 10801741073912 Lot Numbers: NGKT2456 NGKT3292 NGKU0999 NGKU1026 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter A904400A / 00801741074097¿ 10801741074094 Lot Numbers: NGKT3231 NGKU2051 SureStep Intermittent Catheter Tray INTAAI / 00801741183317 10801741183314 Lot Number: NGKU1409

Recalling firm:

C.R. Bard 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.

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

Recall #:

99286

Lot/product code:

Lot Code: Q6 Edge 3 0060650920015*8 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.

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

Recall #:

D-0678-2026

Lot/product code:

Lot: a) 1505121, 1504242, exp 2027-03; 1505132, 1505182, 1505191, 1505291, 1505331, exp 2027-04; b) 1504231, 1504311, exp 2027-03; 1505312, 1505321, exp 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-0686-2026

Lot/product code:

Lot:1505161, 1505181, 1505301, 1505382, exp 2027-04.

Recalling firm:

Bell Pharmaceuticals, Inc

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

Recall #:

98840

Lot/product code:

Catalog Numbers / UDI codes: 899914 / 00801741024801¿ 10801741024808 Lot Number: NGKU4611 899916 / 00801741024818¿ 10801741024815 Lot Numbers: NGKU2448 NGKU4610 899918 / 00801741024825¿ 10801741024822 Lot Number: NGKU3555 ***** SureStep" Foley Tray System with Bardex¿ Lubricath Temp Sensing Foley Catheter REF: A119416M UDI code: 00801741073700 10801741073707 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800361 UDI code: 00801741073939 10801741073936 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A899616 UDI code: 00801741104534¿ 10801741104531 SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter REF: A899914 UDI code: 00801741074004 10801741074001 SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter REF: A899916 UDI code: 00801741074011¿ 10801741074018 SureStep" Foley Tray System Bardex¿ Lubricath¿ Temperature Sensing Catheter REF: A900216 UDI code: 00801741120978¿ 10801741120975 SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter REF: A902914 A902916 A902918 UDI code: 00801741074066¿10801741074063 00801741074073 10801741074070 00801741074080¿10801741074087 Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter REF: 304916 UDI code: 00801741019736 01801741019739 Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter REF: 902916 UDI codes: 00801741024863 10801741024860 (416A) SureStep Foley Tray System Bardex IC Complete Care (714A/716A/718A)SureStep Foley Tray System Bardex IC Complete REF: A304914 A304916 A304918 UDI codes: 00801741104350¿ 10801741104357 00801741104367¿ 10801741104364 00801741100499¿ 10801741100496 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800365 UDI codes: 00801741073960 10801741073967 SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter REF: A899918 UDI codes: 00801741074028 10801741074025 SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter REF: A902618 UDI codes: 00801741104640 10801741104647 SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter REF: A902616 UDI codes: 00801741104633¿ 10801741104630 SureStep Intermittent Catheter Tray REF: INTL16C UDI codes: 00801741183195¿ 10801741183192

Recalling firm:

C.R. Bard Inc

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

Recall #:

D-0681-2026

Lot/product code:

Lot: a) 1505122, 1505343, expires: 2027-04; b) 1505142, 1505341, 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-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.

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

Recall #:

99286

Lot/product code:

Lot Code: R-TRAK 0060650920022*6 K011993 D049085 41875 ITI

Recalling firm:

Pride Mobility Products Corp.

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

Recall #:

H-1241-2026

Lot/product code:

all product with an expiration date prior to Feb 9, 2028 (Best by Date Feb 09, 2028)

Recalling firm:

Publix Super Markets, Inc.

Resolved:

September 4, 2026

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