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Klosterman Baking Company

Klosterman Baking Company Recalls

All product recalls associated with Klosterman Baking Company.

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Recall Summary

Total Recalls

1000

Past Year

353

Class I (Serious)

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 961–980 of 3680 recalls

Cuban Loaf (Klosterman) – Unsanitary Conditions (2022)

Products held under insanitary conditions

Class IIModerate

FDADec 18, 2022IN, OH, TN• Klosterman Baking Company

Seeded Buns (Klosterman) – Unsanitary Conditions (2022)

Products held under insanitary conditions

Class IIModerate

FDADec 18, 2022IN, OH, TN• Klosterman Baking Company

VERIFY Biological Indicators (Steris) – Growth Inconsistency (2022)

Biological indicator (BI) used to promote growth of the G. stearothermophilus and B. atrophaeus spores was inconsistent in promoting growth throughout lot , some BIs within the lot performed as intended while others did not. When used to monitor steam and ethylene oxide sterilization cycles, the potential hazard is that the BI will show no growth indicating that the cycle was effective, even if it may not have been.

1...47 484950 51...184

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Low

FDADec 12, 2022Nationwide• Steris Corporation

VERIFY Steam Test Pack (Steris) – Growth Inconsistency (2022)

Low

FDADec 12, 2022Nationwide• Steris Corporation

Perfusion Tubing Packs (Medtronic) – Temperature Adapter (2022)

An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator either during pre-procedure perfusion set-up or post-procedure when disassembling the perfusion circuit.

Moderate

FDADec 12, 2022Nationwide• Medtronic Perfusion Systems

Affinity Fusion Oxygenator (Medtronic) – Temperature Adapter (2022)

Moderate

FDADec 12, 2022Nationwide• Medtronic Perfusion Systems

Proveo 8 Microscope (Leica) – Power Supply Overheat (2022)

There is a potential issue resulting in the Power Supply potentially becoming overheated due to internal components overstressing. Consequently, due to the overstressing of the internal components, one specific component can fail which will cause the device to unexpectedly shutdown.

High

FDANov 21, 2022Nationwide• Leica Microsystems, Inc.

Provido Microscope (Leica) – Power Supply Overheat (2022)

High

FDANov 21, 2022Nationwide• Leica Microsystems, Inc.

M530 OHX Microscope (Leica) – Power Supply Overheat (2022)

High

FDANov 21, 2022Nationwide• Leica Microsystems, Inc.

Ventana PD-L1 Assay (Ventana) – Light Staining Issue (2022)

Internal comparison studies revealed unacceptable, light staining. Light staining affects the borderline of positive versus negative test results. It can cause a reduction in both staining intensity and the percent positivity, which could potentially lead to a false-negative PD-L1 result.

Moderate

FDANov 18, 2022Nationwide• Ventana Medical Systems, Inc.

Utilimaster Walk-In Van (Utilimaster) – Seat Safety Clip (2022)

Shyft Group is recalling certain 2023 Utilimaster Walk-in vans. The passenger side jump seat may be missing a safety clip that prevents the pivot rod from sliding.

High

NHTSANov 18, 2022Nationwide• UTILIMASTER

Utilimaster Walk-In Van (Utilimaster) – Shock Mount Defect (2022)

Shyft Group (Shyft Group) is recalling certain 2023 Utilimaster Walk-In vans. The retaining nut that holds the shock mount together may have been improperly installed and can loosen.

High

NHTSANov 18, 2022Nationwide• UTILIMASTER

B125M Patient Monitor (GE Medical) – CO2 Measurement Error (2022)

GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that is not at or near sea level.

Moderate

FDANov 16, 2022Nationwide• GE Medical Systems, LLC

B105P Patient Monitor (GE Medical) – CO2 Measurement Error (2022)

Moderate

FDANov 16, 2022Nationwide• GE Medical Systems, LLC

B125P Patient Monitor (GE Medical) – CO2 Measurement Error (2022)

Moderate

FDANov 16, 2022Nationwide• GE Medical Systems, LLC

Utilimaster Aeromaster (Utilimaster) – Side View Display Error (2022)

Shyft Group (Shyft Group) is recalling certain 2022 Utilimaster Aeromaster vehicles. The side-view image may display the wrong side of the vehicle when the turn signal and brake are applied at the same time.

Low

NHTSANov 16, 2022Nationwide• UTILIMASTER

B105M Patient Monitor (GE Medical) – CO2 Measurement Error (2022)

Moderate

FDANov 16, 2022Nationwide• GE Medical Systems, LLC

Vivid q Ultrasound (GE Medical) – Battery Failure (2022)

Fire/Burn Risk

Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.

Moderate

FDANov 10, 2022Nationwide• GE Medical Systems, LLC

Vivid S5 Ultrasound (GE Medical) – Battery Failure (2022)

Fire/Burn Risk

Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.

Moderate

FDANov 10, 2022Nationwide• GE Medical Systems, LLC

Portable Generators (Generac) - Amputation Risk (2022)

This recall involves 6500-watt and 8000-watt Generac portable generators with unit type numbers XT8000E XT8000EFI, GP6500, GP6500E, GP8000E and HomeLink 6500E portable generators, and DR models PRO 6500M and PRO 6500E portable generators. This recall also involves all of these generators listed above purchased after July 29, 2021 through November 3, 2022, containing a repair kit which included full cover handle guards. The generators have gasoline-powered engines that are used to generate electricity for use as backup power. The portable generators have two-wheels and a single, U-shaped, two-grip, flip-up pin-lock handle to help move the generator. Only the following generators are included in this recall. The unit type is identified on the front of the product. The model and serial numbers are printed on a label on the product. Consumers can also check specific unit type, model number, and serial number location information at www.generac.com/service-support/product-support-lookup. Unit Type Model Number First Serial Number Last Serial Number XT8000E G0064330 G0064331 3000037849 3005569372 G0064340 G0064342 XT8000EFI G0071620 G0071621 3003336356 3006597843 G0071621R GP6500 G0076720 G0076800 G0076800R G0076812 G0076830 G0076830R G0076902 G0076902R G0076903 GP6500E G0076820 G0076820R G0076822 GP8000E G0076731 G0076751 G0076751R G0076761 G0076761R G0076861 G0076861R PRO 6500M GP16505DMN GP16505DMNR PRO 6500E GP16505DEN HomeLink 6500E G0068650 G0068651 G0079960

Moderate

CPSCNov 10, 2022Nationwide• Generac Power Systems, of Waukesha, Wisconsin