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Youngstown Grape Distributors, Inc.

Youngstown Grape Distributors, Inc. Recalls

All product recalls associated with Youngstown Grape Distributors, Inc..

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 2741–2760 of 37665 recalls

Focus Greens Juice (Youngstown Grape) – Pasteurization Issue (2024)

Incomplete pasteurization

Class IIModerate

FDAOct 3, 2024AL, AZ, CA +36 more• Youngstown Grape Distributors, Inc.

Watermelon Hydration Juice (Youngstown Grape) – Pasteurization Issue (2024)

Incomplete pasteurization

Class IIModerate

FDAOct 3, 2024AL, AZ, CA +36 more• Youngstown Grape Distributors, Inc.

RENASYS EDGE Pump (Smith & Nephew) – Battery Maintenance Issue (2024)

Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained.

Moderate

FDA

1...136 137138139 140...1884

Page 138 of 1884Next

Oct 2, 2024

AL, CA, CO +10 more

• Smith & Nephew Medical, Ltd.

Legion Oxinium Constrained Femoral Component (Smith & Nephew) – Implant Mislabeling (2024)

Complaint received indicating that a package contained a LGN OX CONSTRAINED FEM 3 LT implant instead of a LGN OX CONSTRAINED FEM 4 LT as described on the product label.

Moderate

FDAOct 2, 2024TX• Smith & Nephew Inc

Genesis II Posterior Stabilized Femoral Component (Smith & Nephew) – Implant Mislabeling (2024)

Complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 5N RIGHT implant instead of a GENESIS II POSTERIOR STABILIZED FEMORAL SIZE 5 LEFT as described on the product label.

Moderate

FDAOct 2, 2024AL, CA, DE +4 more• Smith & Nephew Inc

Legion Oxinium Posterior Stabilized Component (Smith & Nephew) – Implant Mislabeling (2024)

Complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 5N RIGHT implant instead of a GENESIS II POSTERIOR STABILIZED FEMORAL SIZE 5 LEFT as described on the product label.

Moderate

FDAOct 2, 2024AL, CA, DE +4 more• Smith & Nephew Inc

TEMA Elbow Axle (Limacorporate) – Mechanical Behavior Difference (2024)

Due to a potential difference in mechanical behavior between the implanted device and tool(s) used during revision surgery.

Moderate

FDAOct 2, 2024FL, TX• Limacorporate S.p.A Via Nazionale 52 Di San Daniele San Daniele Del Friuli Italy

Spectrum IQ Infusion System (Baxter) – Door Closure Malfunction (2024)

The door on the Spectrum IQ Infusion pump may not be able to fully close.

Moderate

FDAOct 2, 2024GA, ID• Baxter Healthcare Corporation

International HX (INTERNATIONAL) – Fuel Pump Delivery Problem (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International HX and International LT vehicles equipped with Cummins X15 diesel engines. The fuel pump barrels may fracture and cause a fuel leak, resulting in an engine stall.

High

NHTSAOct 1, 2024Nationwide• INTERNATIONAL

Medline Maxorb Extra Alginate Dressing (Advanced Medical) – Packaging Sterility Issue (2024)

Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.

Low

FDAOct 1, 2024Nationwide• Advanced Medical Solutions Ltd. Unit A 33 Road One Winsford United Kingdom

Merlin@home Transmitter with MerlinOnDemand (Abbott) – Software Upgrade Failure (2024)

Due to heart transmitter not being able to upgrade to the current software version in the field after experiencing a power interruption during a prior over-the-wire software download.

Moderate

FDAOct 1, 2024Nationwide• Abbott Medical

Merlin@home Transmitter (Abbott) – Software Upgrade Failure (2024)

Due to heart transmitter not being able to upgrade to the current software version in the field after experiencing a power interruption during a prior over-the-wire software download.

Moderate

FDAOct 1, 2024Nationwide• Abbott Medical

McKesson Calcium Alginate Dressing (Advanced Medical) – Packaging Sterility Issue (2024)

Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.

Low

FDAOct 1, 2024Nationwide• Advanced Medical Solutions Ltd. Unit A 33 Road One Winsford United Kingdom

International CV (INTERNATIONAL) – Air Bag Module Activation Issue (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International CV vehicles. The air bag module may not have been activated during installation.

Moderate

NHTSAOct 1, 2024Nationwide• INTERNATIONAL

Hollister CalciCare Dressing (Advanced Medical) – Packaging Sterility Issue (2024)

Due to defects on primary packaging pouch that compromise the device's ability to maintain a sterile barrier.

Low

FDAOct 1, 2024Nationwide• Advanced Medical Solutions Ltd. Unit A 33 Road One Winsford United Kingdom

Cisplatin Injection (Accord Healthcare) – Impurity Specifications (2024)

Failed Impurities/Degradation Specifications.

Class IIModerate

FDAOct 1, 2024Nationwide• ACCORD HEALTHCARE, INC.

Jack & Green Sprouts Alfalfa & Onion (Jack & The Green Sprouts) – Listeria Contamination (2024)

Listeria

Sprouts may be contaminated with Listeria monocytogenes.

Class IHigh

FDAOct 1, 2024IA, MN, WI• Jack & The Green Sprouts, Inc.

Western Star 49X (WESTERN STAR) – Fuel Pump Delivery Issue (2024)

Daimler Trucks North America, LLC (DTNA) is recalling certain 2025 Freightliner Cascadia, Western Star 49X, Freightliner Custom Chassis XCM and Freightliner Custom Chassis XCP vehicles equipped with certain Cummins fuel pumps. The fuel pump barrels may fracture and cause a fuel leak, which can result in an engine stall.

High

NHTSAOct 1, 2024Nationwide• WESTERN STAR

Jack & Green Sprouts Alfalfa (Jack & The Green Sprouts) – Listeria Contamination (2024)

Listeria

Sprouts may be contaminated with Listeria monocytogenes.

Class IHigh

FDAOct 1, 2024IA, MN, WI• Jack & The Green Sprouts, Inc.

Bard Marquee Biopsy Instrument Kit (Bard) – Needle Retention Defect (2024)

Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle detachment and misplacement, which could lead to tissue damage and bleeding.

Moderate

FDASep 30, 2024Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438