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Publix Super Markets, Inc.

Publix Super Markets, Inc. Recalls

All product recalls associated with Publix Super Markets, Inc..

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Recall Summary

Total Recalls

1000

Past Year

567

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 2841–2860 of 7756 recalls

Steam in Bag Butternut Brussels Pecan (Publix) - Listeria risk (2021)

Listeria

Cubed butternut squash used in the preparation of three of the firm's products is potentially contaminated with Listeria monocytogenes.

Class IIModerate

FDAJan 14, 2021Nationwide• Publix Super Markets, Inc.

Steam in Bag Green Bean Butternut Squash (Publix) - Listeria risk (2021)

Listeria

Cubed butternut squash used in the preparation of three of the firm's products is potentially contaminated with Listeria monocytogenes.

Class IIModerate

FDAJan 14, 2021Nationwide• Publix Super Markets, Inc.

Publix Steam in Bag Butternut Medley (Publix) – Listeria Risk (2021)

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Listeria

Cubed butternut squash used in the preparation of three of the firm's products is potentially contaminated with Listeria monocytogenes.

Class IIModerate

FDAJan 14, 2021Nationwide• Publix Super Markets, Inc.

BEMER INT. AG Austrasse 15 Triesen Liechtenstein: Bemer-Set/ Pro-Set for the following models: REF. 41020...

There potential that electromagnetic fields generated in the therapy system may cause technical defects in a patient using an insulin pumps or a malfunction of a pacemaker.

FDAJan 13, 2021Nationwide• BEMER INT. AG Austrasse 15 Triesen Liechtenstein

Baxter Healthcare Corporation: The PrisMax System Version II Hemodialysis Delivery Syste...

Variability in the performance of the tubing in the ARPS (Automatic Repositioning System) Pump Assembly which may lead to alarm situations during system self-test and therapy. This tubing is normally replaced during annual preventative maintenance. Alarm Situations: During System Self-Test: Alarm code B1215 (ARPS Self-Test failure); During Therapy: B1273 (ARPS Leak), B1215 (ARPS Pressure self-test), B1116 (Return Pressure self-test Failure), B1539 (Access Pod Reposition Failure), B1541 (Effluent Pod Reposition Failure), B1540 (Effluent Filter Pod Reposition Failure). If an alarm occurs, it may lead to delay or interruption of therapy. In the event that therapy is terminated without returning blood to the patient, blood loss may occur.

FDAJan 7, 2021Nationwide• Baxter Healthcare Corporation

Phytonadione Tablets (Bausch) – Impurity Specification (2021)

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

Class IIILow

FDAJan 7, 2021Nationwide• Bausch Health Companies, Inc.

Mephyton Tablets (Bausch) – Impurity Specification (2021)

Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.

Class IIILow

FDAJan 7, 2021Nationwide• Bausch Health Companies, Inc.

Baxter Healthcare Corporation: Infusion Pump

Battery performance issues related to prolonged storage.

FDAJan 6, 2021AL, AK, AZ +49 more• Baxter Healthcare Corporation

Sulfur Ointment (DLC) – Label Mix-Up (2021)

Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.

Class IIModerate

FDAJan 6, 2021Nationwide• DLC Laboratories, Inc

Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland: HAMILTON-H900 Humidifier, Models: 950001, 950004

When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber.

FDAJan 5, 2021CA, FL, NV +3 more• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland

Helena Laboratories, Corp.: Cascade Abrazo aPTT Test Card - Product Usage: are to be ...

Intermittent potential for shorter than expected clot times.

FDAJan 5, 2021Nationwide• Helena Laboratories, Corp.

Metformin Hydrochloride Tablets (Nostrum) – NDMA Impurity (2021)

CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

Class IIModerate

FDAJan 4, 2021Nationwide• Nostrum Laboratories Inc