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CJ Foods Inc., A Division of CJ America

CJ Foods Inc., A Division of CJ America Recalls

All product recalls associated with CJ Foods Inc., A Division of CJ America.

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Recall Summary

Total Recalls

1000

Past Year

579

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 4101–4120 of 10937 recalls

Japanese Style Teriyaki Noodle Bowl (Annie Chun's) - Undeclared Peanuts (2020)

Undeclared Nuts

Pad Thai Noodle Bowl which contains peanuts was packaged with the sleeve for Teriyaki Noodle Bowl leaving undeclared peanuts on the product label.

Class IIModerate

FDAFeb 14, 2020CA, FL, IL +7 more• CJ Foods Inc., A Division of CJ America

DFINE Vertebral Hydraulic Assemblies (Merit Medical) – incorrect expiration date (2020)

Vertebral hydraulic assemblies has incorrect expiration date printed on the labels.The product's shelf-life is two (2) years, but the expiration date printed on the labels is five (5) years.The affected product will begin expiring in March 2020. Using product beyond the validated shelf-life may result in (1) product not functioning as intended and/or (2) a delay in procedure or the need for the procedure to be rescheduled.

Moderate

FDAFeb 13, 2020Nationwide• Merit Medical Systems, Inc.

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DFINE Vertebral Assemblies (Merit Medical) – Incorrect Expiration Label (2020)

Moderate

FDAFeb 13, 2020Nationwide• Merit Medical Systems, Inc.

Open Pivot Aortic Valve Graft (Medtronic) – incorrect label (2020)

Medtronic received a complaint from China that the label on the box for an Open Pivot Heart Valve was labeled as Aortic, but the product was Mitral. The valve itself was correctly labeled as Mitral.

Low

FDAFeb 11, 2020Nationwide• MEDTRONIC ATS MEDICAL, INC.

Banana Pudding Ice Cream (Hunter Farms) – undeclared soy (2020)

Undeclared Soy

The firm was notified that the product contains undeclared soy.

Class IIModerate

FDAFeb 11, 2020IN, NC• Harris Teeter Supermarkets, LLC dba Hunter Farms

SPICE JWH-018 (Carolina Liquid Chemistries) – labeling correction (2020)

Corrections are being made to the device labeling regarding its intended use, to include a statement clarifying it is for research purposes only.

Low

FDAFeb 10, 2020AL, CA, LA +1 more• Carolina Liquid Chemistries Corp

Amoxicillin Tablets (AuroMedics) – Foreign Substance (2020)

Presence of Foreign Substance: Customer complaint of a foreign substance identified as nylon cable tie

Class IIModerate

FDAFeb 7, 2020Nationwide• AuroMedics Pharma LLC

Glycopyrrolate Injection (AuroMedics) – Benzaldehyde Impurity (2020)

Failed Impurities/Degradation Specifications: elevated levels of Benzaldehyde impurity was found in investigative samples (retain samples).

Class IIILow

FDAFeb 7, 2020LA, MS, OH• AuroMedics Pharma LLC

Organic Extra Virgin Coconut Oil (Natural Grocers) – High mold (2020)

Product tested high for mold.

Class IIModerate

FDAFeb 7, 2020AZ, AR, CO +18 more• Vitamin Cottage Natural Food Markets, Inc.

Organic Extra Virgin Coconut Oil (Natural Grocers) – High mold (2020)

Product tested high for mold.

Class IIModerate

FDAFeb 7, 2020AZ, AR, CO +18 more• Vitamin Cottage Natural Food Markets, Inc.

Walk Behind Leaf Blowers (DR Power) – Projectile hazard (2020)

This recall involves DR Walk Behind Leaf Blowers, including DR PREMIER 1200, DR PRO 2000 and DR PRO 2000SP. The blowers are three-wheeled walk behind blowers with an orange circular metal face with a black center with "DR" printed on the front. The model number is printed on the front left side of the main impeller housing and on the serial number label located on the back right side of the main impeller housing. Only the following models are included in the recall: Product name Model Number DR PREMIER 1200 Walk Behind Leaf Blower WB13010DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DMN DR PRO 2000 Walk Behind Leaf Blower WB15020DEN DR PRO 2000SP Walk Behind Leaf Blower WB17020DEN

High

CPSCFeb 6, 2020Nationwide• Country Home Products Inc., d/b/a DR Power Equipment, of South Burlington, Vt.

HEMO-10 Hemospray Hemostat (Wilson-Cook) – handle failure (2020)

Complaints that the handle and/or activation knob on Hemostat devices have cracked or broken when the device is activated. In some cases, this has caused the carbon dioxide cartridge to exit the handle. Most of these complaints reported that the carbon dioxide cartridge exited the handle with minimal force. However, some complaints reported that the carbon dioxide cartridge exited the handle with the potential to project towards a user or a patient.

High

FDAFeb 4, 2020Nationwide• Wilson-Cook Medical Inc.

HEMO-7 Hemospray Hemostat (Wilson-Cook) – handle failure (2020)

High

FDAFeb 4, 2020Nationwide• Wilson-Cook Medical Inc.

TRUMATCH Orthognathics Kit (Materialise) – incorrect plate labeling (2020)

Custom surgical kits contain a plate different than indicated by the package labeling.

Low

FDAFeb 3, 2020NY• Materialise N.V. Technologielaan 15 Heverlee Belgium

ABL90 FLEX Analyzer (Radiometer) – barcode reader error (2020)

The firm received reports of occurrences where the barcode reader misinterpreted the contents of a locally printed barcode label used for entering patient ID or accession number into the analyzer in connection with a sample measurement. This could result is patient mixup and/or lost of sample, resulting in delayed medical treatment.

Moderate

FDAFeb 3, 2020Nationwide• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

ABL90 FLEX PLUS Analyzer (Radiometer) – barcode reader error (2020)

Moderate

FDAFeb 3, 2020Nationwide• Radiometer Medical ApS Akandevej 21 Bronshoj Denmark

TRUMATCH Orthognathic Kit (Materialise) – incorrect plate labeling (2020)

Custom surgical kits contain a plate different than indicated by the package labeling.

Low

FDAFeb 3, 2020NY• Materialise N.V. Technologielaan 15 Heverlee Belgium

UST-2265-2 Probe (Hitachi) – inner cable miswiring (2020)

These 18 probes may have mis-wiring in the inner cables, causing decreased sensitivity and thus resulting in lower peak velocity readings.

Low

FDAJan 31, 2020CA, FL, GA +5 more• Hitachi Medical Systems America Inc

Stealth Spring Clip (Applied Medical) – occlusion failure (2020)

Failure of cardiovascular clips to provide sufficient occlusion of the vessel.

Low

FDAJan 31, 2020Nationwide• Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa

CareLink 2090 Programmer (Medtronic) – cyber vulnerability (2020)

Medtronic Conexus Telemetry has been determined to contain two primary cyber vulnerabilities: improper access control and the cleartext transmission of sensitive information.

Low

FDAJan 30, 2020Nationwide• Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)