Recalls affecting Maryland

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

Recall #:

99023

Lot/product code:

Lot Code: Model Number: 106128 UDI/GTIN 05415067039880 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.

Recalling firm:

Thoratec LLC

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

Recall #:

99023

Lot/product code:

Lot Code: Model Number: 106524US UDI/GTIN 05415067039323 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.

Recalling firm:

Thoratec LLC

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

Recall #:

99023

Lot/product code:

Lot Code: Model Number:106531US UDI/GTIN: 05415067039446 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.

Recalling firm:

Thoratec LLC

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

Recall #:

99023

Lot/product code:

Lot Code: Model Number: 106524US UDI/GTIN 05415067039323 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.

Recalling firm:

Thoratec LLC

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

Recall #:

98913

Lot/product code:

GTIN 00643169090866, Lot Number VA368G3; GTIN 00643169090866, Lot Number VA36V7T; GTIN 00643169936584, Lot Number VA3347Y; GTIN 00643169936584, Lot Number VA33481; GTIN 00643169936584, Lot Number VA33M8V; GTIN 00643169936584, Lot Number VA33M92; GTIN 00643169936584, Lot Number VA33T31; GTIN 00643169936584, Lot Number VA33T33; GTIN 00643169936584, Lot Number VA35B5D; GTIN 00643169936584, Lot Number VA35B5E; GTIN 00643169936584, Lot Number VA35WSP; GTIN 00643169936584, Lot Number VA35WSU; GTIN 00763000963040, Lot Number VA35TTU; GTIN 00763000963040, Lot Number VA35TTV; GTIN 00763000963040, Lot Number VA368FZ; GTIN 00763000963040, Lot Number VA368G3; GTIN 00763000963040, Lot Number VA36V7T; GTIN 00763000963040, Lot Number VA36V8Q; GTIN 00763000968427, Lot Number 0231980220; GTIN 00763000968427, Lot Number 0231980221; GTIN 00763000968427, Lot Number 0231980222; GTIN 00763000968434, Lot Number 0231493884; GTIN 00763000968434, Lot Number 0231493885; GTIN 00763000968434, Lot Number 0231494066; GTIN 00763000968434, Lot Number 0231928923; GTIN 00763000968434, Lot Number 0231929188; GTIN 00763000968434, Lot Number 0231929189; GTIN 00763000968434, Lot Number 0231929192; GTIN 00763000968441, Lot Number 0231367316; GTIN 00763000968441, Lot Number 0231367317.

Recalling firm:

Medtronic Neuromodulation

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

Recall #:

H-0896-2026

Lot/product code:

BEST BY: 27 DEC 26

Recalling firm:

Straus Family Creamery

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

Recall #:

H-0897-2026

Lot/product code:

BEST BY: 30 DEC 26

Recalling firm:

Straus Family Creamery

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

Recall #:

98877

Lot/product code:

Model Number: RFP-400-G; UDI-DI: 00840861102839; 2. Model Number: RFP-401-G; UDI-DI: 00840861102853; 3. Model Number: RFP-402-G; UDI-DI: 00840861102822; 4. Model Number: RFP-404-G; UDI-DI: 00840861102914; 5. Model Number: RFP-407-G; UDI-DI: 00840861102846: 6. Model Number: RFP-456-G; UDI-DI: 00840861102945; All lots produced from January 13, 2025, through lot 26AG02019 on January 13, 2026

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

H-1079-2026

Lot/product code:

LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026

Recalling firm:

Dkiru LLC

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

Recall #:

H-0895-2026

Lot/product code:

BEST BY: 26 DEC 26

Recalling firm:

Straus Family Creamery

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

Recall #:

H-0894-2026

Lot/product code:

QUART - BEST BY: 24 DEC 26; PINT - BEST BY: 25 DEC 26

Recalling firm:

Straus Family Creamery

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

Recall #:

98966

Lot/product code:

UDI-DI: 00643169668911; Serial Numbers: 0232992409 0233010063 0233010115

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

98966

Lot/product code:

UDI-DI: 00763000543679; Serial Numbers: 0231266463 0231468923 0231478249 0231478253 0231478260 0231651627 0231651634 0231651636 0231651637 0231651638 0231651639 0231651641 0231651642

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 #:

H-0893-2026

Lot/product code:

BEST BY: 23 DEC 26; BEST BY: 28 DEC 26

Recalling firm:

Straus Family Creamery

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

Recall #:

D-0554-2026

Lot/product code:

Lot#: AE4013, Exp 1/31/2027; AE5032 & AE5039, Exp 3/31/2028; AE5104, Exp 8/31/2028.

Recalling firm:

Spectra Medical Devices, Llc

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

Recall #:

D-0543-2026

Lot/product code:

Lot M251109, exp Nov 2027

Recalling firm:

ANI Pharmaceuticals, Inc.

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

Recall #:

98877

Lot/product code:

Model Number: RFP-400-G; UDI-DI: 00840861102839; 2. Model Number: RFP-401-G; UDI-DI: 00840861102853; 3. Model Number: RFP-402-G; UDI-DI: 00840861102822; 4. Model Number: RFP-404-G; UDI-DI: 00840861102914; 5. Model Number: RFP-407-G; UDI-DI: 00840861102846: 6. Model Number: RFP-456-G; UDI-DI: 00840861102945; All lots produced from January 13, 2025, through lot 26AG02019 on January 13, 2026

Recalling firm:

Fresenius Medical Care Holdings, Inc.

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

Recall #:

98970

Lot/product code:

GTIN 00840253111012, Lot 38400303, Exp. January 20, 2029

Recalling firm:

Boston Scientific Corporation

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

Recall #:

98963

Lot/product code:

Programmer Model 3650; Software Model 3330; GTIN 05414734509725; Software Versions 25.0.1 - 28.7.1 in the United States (varies based on region)

Recalling firm:

Abbott Medical

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

Recall #:

D-0580-2026

Lot/product code:

Lot HAG2581B, expires: 05/31/2027

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-0548-2026

Lot/product code:

Lot#: 20260310FEN-1, Exp. Date: 09/06/2026

Recalling firm:

IntegraDose Compounding Services LLC

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

Recall #:

98966

Lot/product code:

UDI-DI: 00643169668904, 00613994764379; Serial Numbers: 0232670681 0232709164 0232709168 0232709194 0232709194 0232709199

Recalling firm:

Medtronic Perfusion Systems

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

Recall #:

98978

Lot/product code:

Catalog No. Lot Code T50 SN010 1962242 1964665 2054541 2039361 T50 SN012 1963511 T50 SN020 1971252 1990642 2027441 T50 SN110 1971241 T50 SN115 19647210 T50 SN118 1990631

Recalling firm:

In2bones USA, LLC

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

Recall #:

98990

Lot/product code:

Lot Code: Model 4063 (USA only lead); UDI-DI [4063] 10855728005793; Inspire part number [4063] 900-013-001; serial numbers D53393, D61104 Model 4063 (Global lead); UDI-DI [4063] 10810098650295, Inspire part number [4063] 900-013-003; serial numbers D89539, D89540, D89543, D89559, D89563, D89564, D89577, D8959

Recalling firm:

Inspire Medical Systems Inc.

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

Recall #:

D-0542-2026

Lot/product code:

Lot: KB5Y, Expires: 04/2028; MP4B, Expires: 05/2028; SS4F, Expires: 09/2028.

Recalling firm:

Haleon US Holdings LLC