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Mennel Milling Company

Mennel Milling Company Recalls

All product recalls associated with Mennel Milling Company.

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Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

Most Recent

Dec 2025

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 1181–1200 of 10937 recalls

Bread Flour Unbl Enr (Mennel Milling) – Foreign Material Risk (2024)

Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls

Class IIModerate

FDAJan 30, 2024KY, MI, NJ +3 more• Mennel Milling Company

Pizza 50/50 Unmalted (Mennel Milling) – Foreign Material Risk (2024)

Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls

Class IIModerate

FDAJan 30, 2024KY, MI, NJ +3 more• Mennel Milling Company

Pizza 50/50 Unmalted (Mennel Milling) – Foreign Material Risk (2024)

Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls

Class IIModerate

1...58 596061 62...547

Page 60 of 547Next

FDA

Jan 30, 2024

KY, MI, NJ +3 more

• Mennel Milling Company

Pizza Flour (Mennel Milling) – Foreign Material Risk (2024)

Potential Foreign Material - Metal, Wood, Gasket Material, and/or Sifter balls

Class IIModerate

FDAJan 30, 2024KY, MI, NJ +3 more• Mennel Milling Company

Trinias Angiography System (Shimadzu) – Flat Panel Malfunction (2024)

Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.

FDAJan 29, 2024Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

Vantage MRI Systems (Canon) – SFG Value Mismatch (2024)

For some MRI systems, it has been found that some of the maximum Spatial Field Gradient (SFG) values displayed in "System Information" of the operation window and some of the maximum SFG values described in the safety manual are lower than the correct values, which may cause a patient with an MR conditional device to feel some discomfort during the MR scan.

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

Vantage Elan MRI (Canon) – SFG Value Mismatch (2024)

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

Embrace Drill Tower (Waldemar Link) – Technique Description Mix-up (2024)

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.

FDAJan 29, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Embrace Drill Tower (Waldemar Link) – Technique Description Mix-up (2024)

The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of the instruments.

FDAJan 29, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Vantage Titan MRI (Canon) – SFG Value Mismatch (2024)

FDAJan 29, 2024Nationwide• Canon Medical System, USA, INC.

IdentiTi ALIF System (Alphatec) – Graft Bolt Breakage (2024)

Due to reports of intraoperative graft bolt implantation breakages.

FDAJan 26, 2024Nationwide• Alphatec Spine, Inc. 1950 Camino Vida Roble

I.B.S Compression Screw (In2Bones) – Batch Mix-up (2024)

This Field Action is being conducted following the identification of a batch mix-up between I.B.S Compression screws diameter 6.5mm length 75mm and I.B.S Compression screws diameter 6.5mm length 80mm. The screws of the batches concerned by the recall may have different lengths from those issued on their labels.

FDAJan 26, 2024Nationwide• In2Bones, SAS 28 Chemin du petit Bois Ecully France

BiMobile Dual Mobility System (Waldemar Link) – Mislabeling Risk (2024)

Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery

FDAJan 22, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Vasopressin Injection (IntegraDose) – Sub-potent Drug (2024)

Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.

Class IIModerate

FDAJan 22, 2024MN• IntegraDose Compounding Services LLC

Mexican Style Quinoa Salad (Hans Kissle) – Undeclared Allergens (2024)

Undeclared Soy

contains undeclared soy and egg

Class IHigh

FDAJan 17, 2024ME, MA, NH +2 more• Hans Kissle Company, LLC

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA

HLS Set Advanced (Maquet) – Sterile Barrier Compromise (2024)

The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.

FDAJan 16, 2024Nationwide• Maquet Medical Systems USA