Recalls affecting South Carolina

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

Recall #:

98315

Lot/product code:

Model No. 7303, UDI-DI: 00840095607575, Lot No. 25XXX.

Recalling firm:

Medica Corporation

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

Recall #:

98299

Lot/product code:

1) DYNDTB0529, UDI-DI: 10197344105663(each), 20197344105660(case), Lot Number: All Lot Numbers; 2) DYNDTB1029, UDI-DI: 10197344076956(each), 20197344076953(case), Lot Number: All Lot Numbers; 3) DYNDTB1516, UDI-DI: 10197344105687(each), 20197344105684(case), Lot Number: All Lot Numbers; 4) DYNDTB1530, UDI-DI: 10197344105694(each), 20197344105691(case), Lot Number: All Lot Numbers; 5) DYNDTB1539, UDI-DI: 10197344008254(each), 20197344008251(case), Lot Number: All Lot Numbers; 6) DYNDTB1545, UDI-DI: 10197344098644(each), 20197344098641(case), Lot Number: All Lot Numbers; 7) DYNDTB2045, UDI-DI: 10197344077007(each), 20197344077004(case), Lot Number: All Lot Numbers; 8) DYNDTB0512, UDI-DI: 10197344105656(each), 20197344105653(case), Lot Number: All Lot Numbers; 9) DYNDTB0555, UDI-DI: 10197344105670(each), 20197344105677(case), Lot Number: All Lot Numbers; 10) DYNDTB1022, UDI-DI: 10197344076949(each), 20197344076946(case), Lot Number: All Lot Numbers; 11) DYNDTB1512, UDI-DI: 10197344098613(each), 20197344098610(case), Lot Number: All Lot Numbers; 12) DYNDTB1529, UDI-DI: 10197344098620(each), 20197344098627(case), Lot Number: All Lot Numbers; 13) DYNDTB1537, UDI-DI: 10197344008247(each), 20197344008244(case), Lot Number: All Lot Numbers; 14) DYNDTB1540, UDI-DI: 10197344098637(each), 20197344098634(case), Lot Number: All Lot Numbers; 15) DYNDTB2029, UDI-DI: 10197344076994(each), 20197344076991(case), Lot Number: All Lot Numbers; 16) DYNDTB5077, UDI-DI: 10197344098651(each), 20197344098658(case), Lot Number: All Lot Numbers; 17) DYNDTB1045, UDI-DI: 10197344076963(each), 20197344076960(case), Lot Number: All Lot Numbers; 18) DYNDTB1545D, UDI-DI: 10197344105700(each), 20197344105707(case), Lot Number: All Lot Numbers; 19) DYNDTB2524, UDI-DI: 10197344105717(each), 20197344105714(case), Lot Number: All Lot Numbers; 20) DYNDTB1012, UDI-DI: 10197344076932(each), 20197344076939(case), Lot Number: All Lot Numbers; 21) DYNDTB2012, UDI-DI: 10197344076970(each), 20197344076977(case), Lot Number: All Lot Numbers; 22) DYNDTB2022, UDI-DI: 10197344076987(each), 20197344076984(case), Lot Number: All Lot Numbers; 23) DYNDTB5081, UDI-DI: 10197344098668(each), 20197344098665(case), Lot Number: All Lot Numbers

Recalling firm:

Medline Industries, LP

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

Recall #:

98282

Lot/product code:

Model Number: PDSL6; UDI-DI 00843193113924; Lot 2025-0776;

Recalling firm:

Centinel Spine, Inc.

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

Recall #:

98280

Lot/product code:

Model Number: 1000. UDI Number: (01)00860002987804(17)260228(10)7011098. Lot Number: 7011098. Expiration Date: 02/28/2026.

Recalling firm:

Miach Orthopaedics

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

Recall #:

D-0259-2026

Lot/product code:

Lot # MHA21825, Exp Date: December 31, 2027

Recalling firm:

Alvogen, Inc

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

Recall #:

D-0292-2026

Lot/product code:

Lot #49124, Exp Date 12/31/2026

Recalling firm:

AvKARE

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

Recall #:

D-0352-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0350-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0349-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0346-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0348-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0351-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0347-2026

Lot/product code:

All lots

Recalling firm:

Wizcure Pharmaa Private Limited

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

Recall #:

D-0246-2026

Lot/product code:

Lot #: 19251311, Exp Date April 2027

Recalling firm:

Glenmark Pharmaceuticals Inc., USA

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

Recall #:

98205

Lot/product code:

UDI: 00886874119747, Serial: SQ0326, SQ0336, SQ0341, SQ0345, SQ0346, SQ0356, SQ0367, SQ0368, SQ0375, SQ0377, SQ0379, SQ0380, SQ0386, SQ0387, SQ0389, SQ0394, SQ0395, SQ0398, SQ0401, SQ0404, SQ0412, SQ0413, SQ0415, SQ0419, SQ0420, SQ0422, SQ0425, SQ0427, SQ0428, SQ0432, SQ0433, SQ0436, SQ0443, SQ0447, SQ0448, SQ0451, SQ0454, SQ0457, SQ0458, SQ0462, SQ0464, SQ0469, SQ0470, SQ0662, SQ0727, SQ0740, SQ0761

Recalling firm:

Intuitive Surgical, Inc.

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

D-0256-2026

Lot/product code:

Lot #: AD81290, AD81291, AD81292 and AD81293, Exp. Date 1/31/2027

Recalling firm:

SUN PHARMACEUTICAL INDUSTRIES INC

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

Recall #:

D-0295-2026

Lot/product code:

Lot # S2520304, S2520333, Exp 2/28/2027; S2540186, Exp 4/30/2027

Recalling firm:

Zydus Pharmaceuticals (USA) Inc

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

Recall #:

98244

Lot/product code:

Siemens Material Number (SMN): 11574003; UDI-DI: 04056869993980; Serial Numbers: 170013, 170022, 170023, 170021, 170020, 170025, 170026;

Recalling firm:

Siemens Medical Solutions USA, Inc

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

Recall #:

98242

Lot/product code:

Lot: 7014819/UDI: (01)00850001680196

Recalling firm:

Cerapedics, Inc.

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

Recall #:

98244

Lot/product code:

Siemens Material Number (SMN): 11574002; UDI-DI: 04056869993973; Serial Numbers: 150050, 150035, 150033, 150034, 150048, 150021, 150020, 150053, 150023, 150044, 150049, 150037, 150054, 150011, 150059, 150024, 150038, 150051, 150029, 150045, 150032, 150056, 150043, 150055, 150041, 150026, 150025, 150022, 150031, 150039, 150046, 150042, 150028, 150047, 150030, 150052, 150027, 150057, 150040, 150058, 150063;

Recalling firm:

Siemens Medical Solutions USA, Inc

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

Recall #:

98228

Lot/product code:

All units affected by IFU update. UDI-DI: 1. 8888571562 Cardinal Health Sentinel Seal CDU 50192253003091 (CS) 10192253003093 (EA) 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 50192253003084 (CS) 10192253003086 (EA) 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 50192253003077 (CS) 10192253003079 (EA) 4. 8888571370 Cardinal Health Altitude CDU, Dry Suction, with Easy Change Connector 50192253003039 (CS) 10192253003031 (EA) 5. 8888571299 Cardinal Health Aqua-Seal CDU, Wet Suction 50192253003015 (CS) 10192253003017 (EA) 6. 8888571406 Cardinal Health Aqua-Seal CDU, Wet Suction, Dual Drain 50192253003060 (CS) 10192253003062 (EA) 7. 8888571315 Cardinal Health Aqua-Seal CDU, Wet Suction, with Easy Change Connector 50192253003022 (CS) 10192253003024 (EA) 8. 8884713100 Cardinal Health Thora-Seal Basic CDU, One Chamber, 2000 mL 50192253002643 (CS) 10192253002645 (EA) 9. 1814713105 OUS¿Only - Cardinal Health Thora-Seal Basic CDU, One Chamber, 2000 mL (Bottle only) 50192253002308 (CS) 10192253002300 (CS) 10. 1180571570 OUS¿Only - Cardinal Health Thora-Seal CDU, Two Chamber System, 2600 mL 50192253002292 (CS) 10192253002294 (EA) 11. 8884713308 Cardinal Health Thora-Seal CDU, Three Chamber System, 2500 mL 50192253002650 (CS) 10192253002652 (EA) 12. 8884713900 Cardinal Health Thora-Seal Replacement Collection Chamber, 2500 mL 50192253002667 (CS) 10192253002669 (EA)

Recalling firm:

Cardinal Health 200, LLC

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

Recall #:

D-0265-2026

Lot/product code:

All lots within expiry distributed by Gold Star Distribution.

Recalling firm:

GOLD STAR DISTRIBUTION INC

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

Recall #:

98234

Lot/product code:

ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT, UPC 3014260786847; COLGATE TOOTH BRUSH MED. 12CT, UPC 6001067007289; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct, UPC 808829106879; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct, UPC 808829106886. All codes purchased from this firm

Recalling firm:

GOLD STAR DISTRIBUTION INC

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

Recall #:

98234

Lot/product code:

FIRST AID KIT 24/42PC, UPC 808829102536; LUCKY FIRST AID BANDAGES 24CT, UPC 808829041002. All codes purchased from this firm

Recalling firm:

GOLD STAR DISTRIBUTION INC

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

Recall #:

D-0263-2026

Lot/product code:

All lots within expiry distributed by Gold Star Distribution.

Recalling firm:

GOLD STAR DISTRIBUTION INC