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Old Europe Cheese, Inc.

Old Europe Cheese, Inc. Recalls

All product recalls associated with Old Europe Cheese, Inc..

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Recall Summary

Total Recalls

1000

Past Year

Class I (Serious)

Most Recent

Nov 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 621–640 of 2399 recalls

LA BONNE VIE Cranberry Baked Brie (Old Europe Cheese) – Listeria Risk (2022)

Listeria

potential contamination with Listeria monocytogenes

Class IHigh

FDASep 28, 2022AZ, AR, CA +22 more• Old Europe Cheese, Inc.

TASTE OF INSPIRATION Brie (Old Europe Cheese) – Listeria Risk (2022)

Listeria

potential contamination with Listeria monocytogenes

Class IHigh

FDASep 28, 2022AZ, AR, CA +22 more• Old Europe Cheese, Inc.

Clonidine Hydrochloride Tablets (UNICHEM) – Product Mix-up (2022)

Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,

1...30 313233 34...120

Page 32 of 120Next

Class III

Low

FDASep 19, 2022Nationwide• UNICHEM PHARMACEUTICALS USA INC

Sanitizing Hand Spray (Salon Technologies) – Chemical Contamination (2022)

GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Class IIModerate

FDASep 14, 2022FL, WA• Salon Technologies International Inc

Antica Farmacista Hand Sanitizer (Salon Technologies) – Benzene Risk (2022)

Chemical Contamination: product found to contain benzene

Class IHigh

FDASep 14, 2022FL, WA• Salon Technologies International Inc

Cobas 5800 Instrument (Roche) – False Test Results (2022)

Reported false positive and invalid results on the affected devices due to anomalous baselines. This may lead to erroneous or delayed diagnoses.

FDASep 8, 2022IN• Roche Molecular Systems, Inc.

PTS Cholesterol Strips (PTS Diagnostics) – Instructions Error (2022)

Incorrect instructions for use were packaged into the final product.

FDAAug 16, 2022Nationwide• Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.

Fresenius Medical Care Holdings, Inc.: 2008T and 2008TBluestar Hemodialysis Machines with CDX-I...

(1)Software version 2.74 upgrade and (2)hardware related cause that affects only CDX Machines, has been identified as the UI-MICs Board is sensitive to Electromagnetic Interference (EMI) which will cause the false alarm "Remove USB 2 Device".

FDAJul 27, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed Dissolution Specifications

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Irbesartan Tablets (Jubilant Cadista) – Dissolution Failure (2022)

Failed dissolution specifications.

Class IIModerate

FDAJul 18, 2022Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Roche Diagnostics Operations, Inc.: cobas e801 Immunoassay Analyzer

Software issue resulting in signals and sample test results of Pre-Wash tests being impacted. The following assays are considered impacted by the issue: Anti-HAV2, Anti-HBc IgM, IGF-1, Myogloin, Rubella IgG, and Toxo IgG.

FDAJul 14, 2022Nationwide• Roche Diagnostics Operations, Inc.

Micro Therapeutics, Inc.: Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO...

Outer carton packaging of microcatheters were exposed to wet substance during transport.

FDAJun 30, 2022Nationwide• Micro Therapeutics, Inc.

Micro Therapeutics, Inc.: Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, R...

Outer carton packaging of microcatheters were exposed to wet substance during transport.

FDAJun 30, 2022Nationwide• Micro Therapeutics, Inc.

Za'atar Seasoning (Fuchs) – Salmonella contamination (2022)

Salmonella

The product may be potentially positive for Salmonella due to one of the sub-ingredients (oregano) testing positive for Salmonella.

Class IHigh

FDAJun 27, 2022PA• Fuchs North America, Inc.

Fresenius Medical Care Holdings, Inc.: AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse o...

Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured

FDAJun 21, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Medical Care Holdings, Inc.: AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse os...

Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured

FDAJun 21, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Medical Care Holdings, Inc.: AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 2...

Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the device), potentially harming service technicians and/or other authorized operators. If the ethernet port on the device is touched or manipulated, there is a risk of electrical shock

FDAJun 16, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

Fresenius Medical Care Holdings, Inc.: AquaC UNO H [120V, 60Hz, 1000VA, Fresenius US-Version: ...

FDAJun 16, 2022Nationwide• Fresenius Medical Care Holdings, Inc.

Square D QO Plug-on-Neutral Load Centers (Schneider Electric) - Fire Hazard (2022)

Fire/Burn Risk

This recall involves indoor, outdoor and original equipment manufacturer (OEM) Square D QO Plug-On Neutral Load Centers that were installed in homes, recreational vehicles, or commercial establishments, including restaurants, manufacturing facilities and warehouses, commercial lighting and others. The circuit breaker boxes were sold in gray and come in various sizes (square and rectangular). The recalled circuit breaker boxes were manufactured between February 2020 and January 2022, with date codes between 200561 and 220233. For installed outdoor load centers, the manufacturing date codes are printed on the inside of the cover or door of the unit or on the box itself when the cover or door is open. For installed indoor load centers, a qualified electrician can locate the interior date codes that are not visible to the home owner. Circuit breaker boxes with covers that were manufactured between December 2019 and March 2022 are also included in this recall. The affected catalog/part numbers can be found inside the electrical panel doors for both the U.S. and Canada. Recalled Electrical Panel U.S. and Canada Catalog /Part Numbers CQO116L100PGRB QO130M200PRB QOC30UFWG CQO116M100PRB QO140L200PGRB QOC30UFWGW CQO116M60PRB QO140M200PRB QOC30US CQO124L125PGRB QO142L225PGRB QOC32UF CQO124M100PRB QO142M200PRB QOC32UFW CQO140L200PGRB QO142M225PRB QOC40UF CQO140M200PRB QO1816M200PFTRB QOC40UFW NQC20FWG QO816L100PRB QOC40US NQC20FWGW QOC12UF QOC42UF NQC30FWG QOC12US QOC42UFW NQC30FWGW QOC16UF QOC42US QO112L125PGRB QOC16UFW QOC54UF QO112L200PGRB QOC16US QOC54UFW QO112M100PRB QOC20U100F QOC60UF QO116L125PGRB QOC20U100FW QOCMF30UC QO116M100PRB QOC20U100S QOCMF30UCW QO120M100PRB QOC20UFWG QOCMF42UC QO120M150PRB QOC20UFWGW QOCMF42UCW QO120M200PRB QOC24UF QOCMF54UC QO124L125PGRB QOC24UFW QOCMF54UCW QO124M100PRB QOC24US QOCMF60UC QO124M125PRB QOC30U125C QOCMF60UCW QO130L200PGRB QOC30UF QO130M150PRB QOC30UFW

CPSCJun 16, 2022Nationwide• Schneider Electric USA Inc., of Lexington, Kentucky

Eszopiclone 1mg Tablets (Macleods) – Shortfill Risk (2022)

Shortfill: customer complaints of one to three tablets were reported missing from 30 count bottles.

Class IIModerate

FDAJun 16, 2022Nationwide• Macleods Pharma Usa Inc