Trader Joe&#x27;s Company Recalls

FDAFeb 7, 2024Nationwide• Trader Joe's Company

Cheese Enchiladas Green Sauce (Rico Brands) – Listeria Risk (2024)

Listeria

Firm is recalling enchiladas made with Queso Fresno cheese due to the potential contamination with Listeria monocytogenes.

FDAFeb 7, 2024UT• The Fierro Group Inc. dba Rico Brands

Cheese Enchiladas Red Sauce (Rico Brands) – Listeria Risk (2024)

Listeria

Firm is recalling enchiladas made with Queso Fresno cheese due to the potential contamination with Listeria monocytogenes.

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Class IHigh

FDAFeb 7, 2024UT• The Fierro Group Inc. dba Rico Brands

Roasted Street Corn Salad (Taylor Fresh Foods) – Listeria Risk (2024)

Listeria

Product has the potential to be contaminated with Listeria monocytogenes.

FDAFeb 7, 2024AL, AR, CO +24 more• Taylor Fresh Foods Inc

Southwest Salad (Trader Joe's) – Listeria Risk (2024)

L. mono contamination

FDAFeb 7, 2024Nationwide• Trader Joe's Company

X3 Triathlon CS Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

Azurion 3 (Philips) – Generator Failure Risk (2024)

Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.

FDAFeb 6, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

X3 Triathlon CS Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

X3 Triathlon CS Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

V-MUX Hercules HC Node (Weldon) – Electrical System Risk (2024)

JTEKT is recalling certain Electronic Power Steering Systems. Please see the attached recall report for the affected part numbers. The bolts connecting the electronic power steering unit to the steering rack may be improperly tightened, which can cause the steering gear to lock up and result in a loss of steering control.

NHTSAFeb 6, 2024Nationwide• JTEKT

Azurion 5 (Philips) – Generator Failure Risk (2024)

FDAFeb 6, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

SPII Lubinus Prosthesis (Waldemar Link) – Labeling Confusion (2024)

Due to two complaints, has come to our attention that additional guidance is required on the correct interpretation of the carton label Size and Type columns to avoid misinterpretation during surgery.

Low

FDAFeb 6, 2024Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

X3 Triathlon CS Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

Triathlon TS Plus Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

Azurion 7 (Philips) – Generator Failure Risk (2024)

FDAFeb 6, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Triathlon TS Plus Insert (Howmedica) – Packaging Breach (2024)

Potential packaging breaches of inner blister and outer sterile blister.

FDAFeb 6, 2024Nationwide• Howmedica Osteonics Corp.

Sustain Herbal Supplement (Today The World) – Undeclared Tadalafil (2024)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this drug an unapproved drug.

FDAFeb 6, 2024Nationwide• Today The World

Arize Herbal Supplement (Today The World) – Undeclared Nortadalafil (2024)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.

FDAFeb 6, 2024Nationwide• Today The World

SCHWINNNG Herbal Supplement (Today The World) – Undeclared Nortadalafil (2024)

Undeclared Allergen