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Lins Waha International Corp

Lins Waha International Corp Recalls

All product recalls associated with Lins Waha International Corp.

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Recall Summary

Total Recalls

1000

Past Year

144

Class I (Serious)

154

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 141–160 of 1339 recalls

Farmer House Olive Strips (Lins Waha) – Contains Cyclamates (2025)

Contains Cyclamates

Class IIILow

FDAMar 11, 2025AL, FL, GA +15 more• Lins Waha International Corp

Daily Veggies Enoki Mushroom (New Age) – Listeria Contamination (2025)

Listeria

Contaminated with Listeria monocytogenes

Class IHigh

FDAMar 11, 2025IN, NY• New Age International, Inc.

Calais Grape Jelly (Elwood) – Undeclared Colors (2025)

Undeclared Allergen

Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)

Class III

1...6 789 10...67

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Low

FDAFeb 19, 2025NJ, NY• Elwood International, Inc.

Madras Curry Powder (Trong Food) – Lead Contamination (2025)

Elevated levels of lead 5.48mg/kg and 2.59mg/kg in (2) lots of Madras Curry Powder.

Class IIModerate

FDAJan 28, 2025IN, MD, WA +1 more• Trong Food International

Extra Virgin Olive Oil (Daniele) – Incorrect Oil (2025)

Product is likely Canola Oil, not Extra Virgin Olive Oil

Class IIILow

FDAJan 6, 2025NY• D.F.S. International, Ltd.

Daily Veggies Enoki Mushroom (New Age International) – listeria risk (2024)

Listeria

may be contaminated with Listeria monocytogenes

Class IHigh

FDADec 11, 2024MD, NY• New Age International, Inc.

International EMV (International) – Defroster Circuit Breaker Missing (2024)

International Motors, LLC (International) is recalling certain 2025 EMV vehicles. A circuit breaker may be missing, causing the defrosting system to be inoperative. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 103, "Windshield Defrosting and Defogging Systems."

High

NHTSADec 3, 2024Nationwide• INTERNATIONAL

International HX (International) – Brake Release Delay (2024)

International Motors, LLC (International) is recalling certain 2022-2025 HX vehicles. The service brake may take longer than expected to release. As such, these vehicles may fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."

High

NHTSANov 21, 2024Nationwide• INTERNATIONAL

Kirkland Severe Cold & Flu (LNK) – Quality Control Issue (2024)

CGMP Deviations: Released product should have been rejected.

Class IIModerate

FDANov 14, 2024Nationwide• LNK International, Inc.

Diabetics Foot Cream (Brands International) – Inadequate Testing (2024)

CGMP Deviations: lack of adequate release testing.

Class IIModerate

FDANov 13, 2024Nationwide• Brands International Corporation

2025 International HX (International) – Axle Lubrication Issue (2024)

International Motors, LLC (International) is recalling certain 2024-2025 HX vehicles. An insufficient amount of lubricant in the front steer drive (FSD) axle hubs may result in damage to the wheel bearings.

High

NHTSANov 4, 2024Nationwide• INTERNATIONAL

2025 International HV (International) – software communication issue (2024)

International Motors, LLC (International) is recalling certain 2021-2024 Lonestar, 2021-2025 RH, HV, MV, LT, HX, and 2022 PROSTAR vehicles, equipped with Bendix EC80 Advanced Electronic Control Units (ECU). Electrical noise and low signal to the power line carrier may cause the ECU to incorrectly process commands or stop working.

High

NHTSAOct 31, 2024Nationwide• INTERNATIONAL

Chlorpheniramine Tablets (BLI) – Stability Assay Issue (2024)

Superpotent Drug: Stability failure for assay at 6 months test time-point.

Class IIModerate

FDAOct 21, 2024MO, OH• BLI International, Inc.

DRG:HYBRiD-XL Insulin (DRG International) – Recalibration Failure (2024)

The user of the assay may either face a failure message during re-calibration of the Hybrid.XL instrument using the re-calibration R1 and R2 of the device or find controls out of specification (failed Control High) which causes a delay in results.

Low

FDAOct 7, 2024Nationwide• DRG International, Inc.

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

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

17-OH Progesterone ELISA Kit (DRG) – Control Range Mismatch (2024)

The High and Low Control acceptance ranges in the Certificate of Analysis (CofA) did not match the acceptance range information on the High and Low Control Component labels. Due to the defect, the device failed to provide results, which may result in a delay in obtaining test results and a remote chance of an adverse health risk.

Moderate

FDASep 13, 2024AZ, CA, GA +1 more• DRG International, Inc.

AirJet HydroJet Spa Pumps (Bestway) – Fire Hazard (2024)

Fire/Burn Risk

The spa pumps could have been sold separately, or in a package with an inflatable spa liner in different colors, styles, and inflatable spa sizes. The inflatable spa liners packaged with the pumps are sold under the brand names SaluSpa, Coleman, and Hydro-Force, which are printed on the side of the liner. This recall only includes AirJet and HydroJet Spa Pump model numbers P05332, P05339, P05711, P05807, P07000, P07001, P05511, P07034, and P07572. "Bestway" and the model number are printed on the label on the side or back of the spa pump.

High

CPSCSep 12, 2024Nationwide• Bestway (Hong Kong) International Ltd., of China

J-Basket Napa Kimchi (JFC International) – yeast growth (2024)

High levels of Yeast growth and film on top of jarred Kimchi product.

Class IIModerate

FDAAug 1, 2024AZ, CO, FL +7 more• J F C International Inc

CustomEyes Procedure Packs (Beaver Visitec) – Syringe Recall (2024)

Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes manufactured by Sol-M are present in some of BVI CustomEyes Procedure Packs.

High

FDAJul 26, 2024Nationwide• Beaver Visitec International, Inc.