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Harris Teeter Supermarkets, LLC dba Hunter Farms

Harris Teeter Supermarkets, LLC dba Hunter Farms Recalls

All product recalls associated with Harris Teeter Supermarkets, LLC dba Hunter Farms.

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Recall Summary

Total Recalls

1000

Past Year

589

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 4761–4780 of 10393 recalls

Smooth & Creamy Take the Cake Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Harris Teeter Chocolate Ice Cream – Undeclared Soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Fresh Market Mint Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

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Class II

Moderate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Mint Chocolate Chip Ice Cream (Harris Teeter) – undeclared soy (2019)

The firm discovered that the allergen soy was not declared in the ingredient statement or allergen declaration.

Class IIModerate

FDAOct 17, 2019AL, NC, VA• Harris Teeter Supermarkets, LLC dba Hunter Farms

Scenaria CT System (Hitachi) – Cable Attachment Risk (2019)

There is a possibility that the cables to the controller unit may not be affixed properly, creating the potential for a cable to detach during scanning and eject from the system.

Moderate

FDAOct 16, 2019CA, FL, GA +13 more• Hitachi Medical Systems America Inc

HeartStart XL+ Defibrillator (Philips) – Switch Failure Risk (2019)

The rotary therapy selector switch may fail, resulting in unexpected device behavior. These behaviors include: The device may not turn on; The device may not perform the selected function; The device may deliver a shock with an energy level different from the setting selected by the user.

High

FDAOct 16, 2019Nationwide• Philips North America, LLC

Giraffe Incubator Carestation (GE Healthcare) – panel closure risk (2019)

Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.

High

FDAOct 11, 2019Nationwide• GE Healthcare, LLC

Giraffe Incubator (GE Healthcare) – panel closure risk (2019)

Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.

High

FDAOct 11, 2019Nationwide• GE Healthcare, LLC

Giraffe OmniBed (GE Healthcare) – panel closure risk (2019)

Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.

High

FDAOct 11, 2019Nationwide• GE Healthcare, LLC

Giraffe OmniBed Carestation (GE Healthcare) – panel closure risk (2019)

Giraffe Incubator, Giraffe OmniBed, Giraffe Incubator Carestation, and Giraffe OmniBed Carestation Bedside panels and portholes can appear closed without being latched. Potential patient fall.

High

FDAOct 11, 2019Nationwide• GE Healthcare, LLC

Atellica CH 930 Analyzer (Siemens) – barcode scanning issue (2019)

On the Atellica CH 930 Analyzer, when scanning barcodes at the module console for Integrated Multisensor Technology (IMT) system fluids (Standard A (Std A) and Standard B (Std B)) for Sodium (Na), Potassium (K), and Chloride (Cl), the system will translate the decimal point separators to commas. This will result in invalid concentration values for the fluids, therefore the system will utilize default nominal values instead of lot specific IMT fluid concentration values for calculation of the calibrations and results for the Na, K, and Cl methods.

Moderate

FDAOct 11, 2019Nationwide• Siemens Healthcare Diagnostics, Inc.

Encina HA Femoral Stem (Signature Orthopaedics) – mislabeled packaging (2019)

The firm has identified that packaging containing components of the hip replacement range are mislabeled. This could result in the product intended to be used for a procedure not included in the packaging resulting in a surgical delay.

Low

FDAOct 9, 2019CA• Signature Orthopaedics Europe Ltd Unit A, IDA Business & Technology Park Garrycastle Athlone Ireland

Amino Acid Injection (Nephron) – Sterility and Leak Risk (2019)

Lack of Assurance of Sterility; bags have potential to leak

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

PF-Fentanyl Citrate (Nephron) – Glass Contamination (2019)

GMP Deviations: potential glass contamination

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

del Nido Cardioplegia Solution (Nephron) – Sterility and Leak Risk (2019)

Lack of Assurance of Sterility; bags have potential to leak

Class IIModerate

FDAOct 9, 2019Nationwide• Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Thor Citation (Thor Motor Coach) – label compliance (2019)

Thor Motor Coach (TMC) is recalling certain 2014 Tuscany 36M, 40E, 2015 Citation 24SL, Siesta 24SL, Axis 25.1 and Vegas 25.1, 2016 Four Winds 31E, 31W, 35SF, Chateau 31E, 31W, Synergy SD24, Citation 24SL, 24SS and Siesta 24SL, 24SS, 2017 Four Winds 31E, 31W, Chateau 31E, 35SD, Citation 24SS and Siesta 24SS, 2018 Citation 24SS and Siesta 24SS, 2019 Quantum CR24, Four Winds 24BL, Citation 24MB and Siesta 24MB and 2020 Quantum CR24, Citation 24MB, Siesta 24MB, Chateau 24BL and Synergy 24MB vehicles. The Occupant and Cargo Carrying Capacity (OCCC) label has the incorrect carrying capacity listed, which can allow the vehicle to be overloaded. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other Than Passenger Cars."

Moderate

NHTSAOct 8, 2019Nationwide• THOR MOTOR COACH

Lag Screw Guide Pin Sleeve (Smith & Nephew) – manufacturing error (2019)

LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing error. The detent balls in the guide pin sleeve were not drilled to the correct depth, which will cause them to not fully compress.

Moderate

FDAOct 7, 2019Nationwide• Smith & Nephew, Inc.

Prismaflex Control Unit (Baxter) – Communication Error Risk (2019)

Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.

Moderate

FDAOct 4, 2019Nationwide• Baxter Healthcare Corporation

HeartStart XL+ Monitor (Philips) – Device Restart Issue (2019)

Device may fail to turn on or unexpectedly attempt to restart, rendering it unable to return to a ready for use state. Additionally, this issue may occur when the device is in standby mode, when attempting to power on to run a self-test. If this occurs, the device will indicate that it is not ready for use.

Moderate

FDAOct 3, 2019Nationwide• Philips North America, LLC

CareLink Programmer (Medtronic) – Longevity Estimate Error (2019)

There is a potential for Medtronic programmer and remote monitoring software applications to display an inaccurate remaining longevity estimate for a subset of implanted cardiac device models. This issue does not impact device functionality.

Moderate

FDAOct 3, 2019Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)