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Twin Sisters Creamery, LLC

Twin Sisters Creamery, LLC Recalls

All product recalls associated with Twin Sisters Creamery, LLC.

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Recall Summary

Total Recalls

1000

Past Year

937

Class I (Serious)

125

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 61–80 of 17592 recalls

Twin Sisters Mustard Seed Cheese (Twin Sisters Creamery) – E. coli Contamination (2025)

E. coli

Raw milk Mustard Seed cheese is recalled due to E. coli O103:H2 and E. coli O74:H25.

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Twin Sisters Whatcom Blue Cheese (Twin Sisters Creamery) – E. coli Risk (2025)

E. coli

Raw milk Whatcom Blue cheese is recalled due to E. coli O103:H2.

Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Twin Sisters Farmhouse Cheese (Twin Sisters Creamery) – E. coli Contamination (2025)

E. coli

Raw milk Farmhouse cheeses are recalled due to E. coli O103:H2 and E. coli O74:H25.

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Class IHigh

FDAOct 24, 2025IN, OR, WA• Twin Sisters Creamery, LLC

Senographe Pristina (GE Medical) – X-Ray Warning Label Missing (2025)

Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR 1020.30(j).

Moderate

FDAOct 24, 2025Nationwide• GE Medical Systems, LLC

LEACHOI Bed Rail (Mobility Source) – Entrapment Risk (2025)

This recall involves LEACHOI Bed Rails, ASIN B0BZVCG2R5. The bed rail comes in black/silver and weighs 7.72 pounds. The product measures 15.6 inches by 25.4 inches by 24 inches.

Very High

CPSCOct 23, 2025Nationwide• Mobility Source Medical Technology Co., Ltd, of China

Ice Cream Factory Graham Pieces – Foreign Material Risk (2025)

Foreign material fragments consisting of aluminum foil and packaging material were identified in brown sugar ingredient that may have been used in the products

Class IIModerate

FDAOct 23, 2025AL, AR, FL +26 more• Ice Cream Factory, LLC

CareLink Clinic (Medtronic) – Graph Data Inaccuracy (2025)

Software error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based on the incorrect data displayed on the 24-hour sensor glucose overview graph may lead to hypoglycemia or hyperglycemia.

Moderate

FDAOct 21, 2025Nationwide• Medtronic MiniMed, Inc.

Opdualag Injection (Bristol-Myers Squibb) – Sterility Concern (2025)

Lack of Assurance of Sterility.

Class IIModerate

FDAOct 21, 2025Nationwide• Bristol-Myers Squibb Company

Sevoflurane V90 Vaporizer (Mindray) – Anesthesia Leakage Risk (2025)

Potential for anesthesia leakage.

Moderate

FDAOct 20, 2025Nationwide• Mindray DS USA, Inc. dba Mindray North America

HR-ACT Cartridges (Medtronic) – External Label Contamination (2025)

Medtronic personnel observed trace amounts of dry blood on the external carton label and Instructions for Use (IFU) in five boxes of one lot of ACT Cartridges.

Low

FDAOct 20, 2025Nationwide• Medtronic Perfusion Systems

Isoflurane V90 Vaporizer (Mindray) – Anesthesia Leakage Risk (2025)

Potential for anesthesia leakage.

Moderate

FDAOct 20, 2025Nationwide• Mindray DS USA, Inc. dba Mindray North America

IntelePACS (Intelerad) – Software Communication Bug (2025)

Software application that receives digital images and data to be communicated, processed, manipulated, enhanced, stored, displayed has a bug that could cause data loss in Relevant Clinical Info field when modifying studies through Case Editor in either Technologist Portal or Referring Physician Portal, which could result in loss of clinical information, which could impact clinical decision-making.

Moderate

FDAOct 17, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

MAHURKAR Catheter Tray (Mozarc) – Packaging Seal Integrity (2025)

A potential issue with the seal integrity of header bag packaging.

Low

FDAOct 17, 2025Nationwide• Mozarc Medical US LLC

Multichem ID-B (Techno-Path) – HBsAg Recovery Issue (2025)

Potential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform.

Moderate

FDAOct 17, 2025CA, CO, CT +14 more• TECHNO-PATH MANUFACTURING LTD. Fort Henry Business Park Ballina Tipperary Ireland

EZDilate Nephrostomy Catheter (Olympus) – Incorrect Balloon Size (2025)

Device kits contained an incorrectly sized 4mm x 4cm urinary tract balloon catheter (BURS0404) instead of the correct 8mm x 15cm nephrostomy tract balloon catheter (BPCN0815). All other components in the kits were correctly included and packaged in the kit.

Moderate

FDAOct 17, 2025AK, CA, IA +3 more• Olympus Corporation of the Americas

VANTAGE GALAN 3T (Canon Medical) – Electrode Distance Compliance (2025)

Affected system contains components that do not meet the required distance between electrodes for compliance with the IEC 60601-1 standard for medical electrical equipment.

Moderate

FDAOct 16, 2025NV, OH• Canon Medical System, USA, INC.

Ceiling Type X-Ray Tube Support (Shimadzu) – Mounting Shaft Risk (2025)

Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.

High

FDAOct 16, 2025Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

Beckman Coulter Bicarbonate Reagent (Beckman) – Result Interference (2025)

Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.

Moderate

FDAOct 14, 2025Nationwide• Beckman Coulter Ireland, Inc. Lismeehan O'Callaghan'S Mills Ireland

EVIS EXERA III Duodenovideoscope (Olympus) – Reprocessing Update (2025)

Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes, reminding users to closely follow the operation and reprocessing instructions, and providing updated materials to users.

Moderate

FDAOct 14, 2025Nationwide• Olympus Corporation of the Americas

BD Luer Tip Caps (Becton Dickinson) – Biocompatibility Failure (2025)

BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.

Moderate

FDAOct 14, 2025Nationwide• Becton Dickinson & Company