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The Little Oak Company Ltd

The Little Oak Company Ltd Recalls

All product recalls associated with The Little Oak Company Ltd.

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Recall Summary

Total Recalls

1000

Past Year

582

Class I (Serious)

Most Recent

Dec 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 1441–1460 of 10937 recalls

LittleOak Infant Formula (Little Oak) – Regulatory Issue (2023)

No pre-market notification and Mixing instructions not in ounces

Class IIModerate

FDASep 11, 2023AL, AK, AR +43 more• The Little Oak Company Ltd

Organic Raw Walnuts (Lipari Foods) – Undeclared cashews (2023)

Undeclared Allergen

Undeclared cashews

Class IIModerate

FDASep 9, 2023FL, IL, IN +3 more• Lipari Foods Operating Company, LLC.

Omega Monitor Suspension (Omega Medical) – Boom Detachment (2023)

An actuator separated from the pivot mechanism on a lower monitor boom system column. The lower boom became detached at the point shown and was restrained by the installed safety cable.

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Moderate

FDASep 8, 2023AL, CA, IL +8 more• Omega Medical Imaging, Inc.

F2-01 Patient Monitor (GE Medical) – Data Communication Interruption (2023)

There is a potential interruption of data communication between E-modules inserted in the F2-01 Frame and CARESCAPE ONE and CARESCAPE Canvas 1000 patient monitors if the F2-01 Frame has not been powered down within the last 120 days.

Moderate

FDASep 8, 2023Nationwide• GE Medical Systems China Co., Ltd. National Hi-Tech No.

Commercial Clothes Dryers (Whirlpool) – Fire hazard (2023)

Fire/Burn Risk

This recall involves all ADC brand stacked commercial clothes dryers with a 30 lb. capacity and model number ADG-30X2R or ADG-30X2Ri. Both models were sold in on-premise and coin-operated configurations for multi-unit housing, laundromats, and other facilities that use commercial laundry equipment. Logos and branding may appear differently depending on when the unit was manufactured. The model number for each unit is printed inside near the hinges of the upper door. The ADG-30X2R units were also sold in custom colors other than white to fit location branding.

High

CPSCSep 7, 2023Nationwide• Whirlpool Corporation, of Benton Harbor, Michigan

RX Monaco Analyzer (Randox) – Rerun Setting Failure (2023)

RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for Auto reruns, not meeting sample re-run conditions when samples are above or below assay range and may result i issues with the re-run feature conditions when incorrectly. Potential to report incorrectly.

Moderate

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Venue Go Standard Cart (GE Medical) – Tilt Mechanism Failure (2023)

Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling.

High

FDASep 6, 2023Nationwide• GE MEDICAL SYSTEMS, ISRAEL LTD. Nativ Haa??or Street no.

RX Daytona Plus Clinical Chemistry Analyzer (Randox) – rerun settings issue (2023)

Moderate

FDASep 6, 2023Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

AU/DxC Chemistry Transferrin (Beckman Coulter) – stability claims issue (2023)

The firm has identified that the Transferrin reagent does not meet the Instructions for Use (IFU) reagent on-board stability claims, which may cause control failures and/or erroneous patient samples results. The Complaint handling unit has received a total of 2 safety cases (CASE-2023-02027212 and CASE-2023-02045278) and 99 quality cases with the failure mode attributed to Transferrin reagent (OSR6152 / lot 2573) associated with reagent blank shifts for the Reagent 2 (R2), imprecision, calibration failures, erratic Quality Control (QC) recoveries, and/or erroneous high/low (serum, plasma, urine) patient results. The issue was confirmed through internal testing by Beckman Coulter on June 30, 2023. Reagent Blank shifts for R2, imprecision, calibration failures, erratic Quality Control (QC) recoveries, and/or erroneous high/low (serum, plasma, urine) patient results. The issue was confirmed through internal testing by Beckman Coulter on June 30, 2023.

Moderate

FDASep 6, 2023Nationwide• Beckman Coulter Biomedical Division Lismeehan, O'Callaghan's Mills County Clare Ireland

Roasted Salted Pecan Halves (Lipari Foods) – Mislabeled nuts (2023)

Top label says Roasted Salted Pecan Halves, but product is actually filberts / hazelnuts

Class IIModerate

FDASep 6, 2023FL, IL, IN +5 more• Lipari Foods Operating Company, LLC.

Life Is Peachy Ice Cream (Life Raft) – Listeria contamination (2023)

Listeria

South Carolina Department of Health discovered the product contained Listeria monocytogenes.

Class IHigh

FDASep 5, 2023DC• Life Raft Treats Ice Cream Factory

Ice Cream Not Fried Chicken (Life Raft) – Listeria contamination (2023)

Listeria

South Carolina Department of Health discovered the product contained Listeria monocytogenes.

Class IHigh

FDASep 5, 2023DC• Life Raft Treats Ice Cream Factory

Guardian System (Angel Medical) – premature service end (2023)

Device reaching End of Service prematurely.

High

FDASep 1, 2023Nationwide• Angel Medical Systems, Inc.

LAVH Pack (American Contract) – component investigation (2023)

During an internal investigation, ACS identified that the components, I.V. Cath (part number 4252535-02) and Adhesive Dermabond (part number DHVM12) were inadvertently subjected to the ACS sterilization process and exposed to EO and higher temperatures than approved by the component manufacturer. As a result, the components may (1) have a loss/lack of functionality, (2) loss of drug efficacy, if applicable, and (3) have higher than specified EO residuals.

Moderate

FDASep 1, 2023Nationwide• American Contract Systems, Inc.