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Hy-Vee, Inc. dba Hy-Vee Fresh Commissary

Hy-Vee, Inc. dba Hy-Vee Fresh Commissary Recalls

All product recalls associated with Hy-Vee, Inc. dba Hy-Vee Fresh Commissary.

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Recall Summary

Total Recalls

1000

Past Year

891

Class I (Serious)

124

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 3661–3680 of 17593 recalls

HyVee Oven Baked Beans (Hy-Vee) – potassium sorbate excess (2022)

Baked bean product contains excessive amount of potassium sorbate

Class IIILow

FDAJun 28, 2022IL, IN, IA +6 more• Hy-Vee, Inc. dba Hy-Vee Fresh Commissary

ChemoLock Bag Spike (ICU Medical) – Port Connection Variation (2022)

Ports have a potential for unintended disconnection, inability to connect to or fully engage with injectors, due to a variation in the spring inside the Port, which may cause delay of therapy and exposure to caustic substances. Ports available as standalone connectors, or utilized as access points on vial adaptors, bag spikes, and administration sets.

Moderate

FDAJun 27, 2022Nationwide• ICU Medical, Inc.

Nifedipine WSP Ointment 0.2% (Valor Compounding) – Potency Issue (2022)

Subpotent and Superpotent Drug

1...182 183184185 186...880

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Class I

High

FDAJun 27, 2022CA• Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy

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.

Ambra PACS Software (DICOM Grid) – Patient Information Edit Issue (2022)

A race condition between the storage system and services database has the potential to revert edits made to patient information upon first ingestion of a study.

Moderate

FDAJun 23, 2022AR, CA, CO +40 more• DICOM Grid, Inc. d/b/a Ambra Health

Coda Pendant Light Fixtures – impact injury risk (2022)

The recalled Coda pendant is a clear or smoke glass suspended light fixture that provides general illumination and is available in two sizes, large (40" high and weighs 7 lbs.) and small (21" high and weighs 4 lbs.). The model/item number is on the light fixture packaging. The light uses an integrated LED light source. The recall involves the following model numbers: Item Number Description 700TDCDAPLCCS-LED930 Coda Large, Clear Glass 700TDCDAPLKCS-LED930 Coda Large, Smoke Glass 700TDCDAPSCCS-LED930 Coda Small, Clear Glass 700TDCDAPSKCS-LED930 Coda Small, Smoke Glass 365TDMISC4052 Custom spare part LED module with 20' cord 365TDCODALS-A Spare part LED module

Moderate

CPSCJun 23, 2022Nationwide• Guangzhou Xiongyi Precision Metalworking Co. Ltd., of China

Crome Implantable Cardioverter Defibrillator (Medtronic) – Reduced Shock Energy (2022)

There is the potential for reduced shock energy (~79% of programmed energy) during high-voltage (HV) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).

Moderate

FDAJun 22, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Cobalt Implantable Cardioverter Defibrillator (Medtronic) – Reduced Shock Energy (2022)

Moderate

FDAJun 22, 2022Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Randox Cholesterol Test (Randox) – Performance Calibration Issue (2022)

Product fails to meet the performance claims quoted on the kit insert: Manual Procedure when calibrating using the standard provided in the kit, the change in absorbance is lower than expected generating internal quality control results high outside range; Cholesterol (CHOL) Instrument Specific Application using the recommended calibration material CAL2351, the product fails to meet its linearity performance claim quoted on the kit inserts. The linearity is reduced by up to -35% however Quality Control results will still fall within assigned ranges. This may lead to delayed results.

Moderate

FDAJun 22, 2022Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Blue Kuna Taste of Devil's Night Heat BBQ Sauce (FEAST Detroit) – mislabeled vegan (2022)

The product was mislabeled as Vegan Product but contains anchovies

Class IIModerate

FDAJun 21, 2022MI• Food Entrepreneur Accelerator and Startup Terminal, DBA FEAST Detroit

BD Intraosseous Needle Kit (Bard Access) – Stylet Removal Risk (2022)

BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss of intraosseous access; 2) Stylet safety mechanism may not engage as the stylet is removed; 3) Metal discs in the powered driver may stick rendering the driver unusable.

Moderate

FDAJun 20, 2022Nationwide• Bard Access Systems, Inc.

Merlin 2 PCS Programmer (St. Jude Medical) – Programming System Design (2022)

The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical devices during implant and follow-up.

Low

FDAJun 17, 2022AL, AK, AZ +49 more• St. Jude Medical, Cardiac Rhythm Management Division

Merlin PCS Programmer (St. Jude Medical) – Software Display Error (2022)

There is a potential for programmer software (Merlin PCS) and remote monitoring software application (Merlin.net) to display overestimated predicted battery longevity for certain pacemakers.

Low

FDAJun 17, 2022AL, AK, AZ +49 more• St. Jude Medical, Cardiac Rhythm Management Division