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ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc. Recalls

All product recalls associated with ARROW INTERNATIONAL Inc..

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Recall Summary

Total Recalls

1000

Past Year

135

Class I (Serious)

159

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 161–180 of 1146 recalls

UltraFlex IAB Catheter Kit (Arrow) – Health Consequence (2024)

Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic balloon to completely inflate over its full length -damaged or broken central lumen in the segment contained within the balloon -helium loss or blood in the helium pathway.

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.

FiberOptix IAB Catheter Kit (Arrow) – Health Consequence (2024)

FDAApr 29, 2024Nationwide• ARROW INTERNATIONAL Inc.

Organic Black Chia Seeds (Walmart) – Salmonella Risk (2024)

1...7 8910 11...58

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Salmonella

Salmonella contamination

Class IHigh

FDAApr 15, 2024AL, CA, CO +9 more• NATURAL SOURCING INTERNATIONAL,LLC

International Bread Pita Chips – Incomplete Wheat Labeling (2024)

Label declares flour as an ingredient but does not declare sub-ingredients (wheat).

Class IIModerate

FDAApr 5, 2024CA• INTERNATIONAL PITA BREAD, INC.

International Bread Pita Chips – Incomplete Wheat Labeling (2024)

Label declares flour as an ingredient but does not declare sub-ingredients (wheat).

Class IIModerate

FDAApr 5, 2024CA• INTERNATIONAL PITA BREAD, INC.

L-Series Fire Alarm Sounders (Honeywell) – Safety Malfunction (2024)

Fire/Burn Risk

This recall involves all Honeywell System Sounder L-series Low Frequency Sounders, Sounder Strobes, and Compact Sounders. The sounder and strobes are square, with white and red plastic housings, listed for wall mounting and measure about 5.6 by 4.7 inches for the sounders and strobes and about 5.3 by 3.5 inches for the compact sounder. The model number, date codes and "System Sensor" are printed on the product label and carton. Date codes 3034 and 3035 and the following models are included in this recall: HWL-LF, HWL-LF-BP10, HRL-LF, HRL-LF-BP10, HGWL-LF-BP10, P2WL-LF.

CPSCMar 14, 2024Nationwide• Honeywell International Inc., of Charlotte, North Carolina

International LT (International) – Taillight Wiring Error (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International LT vehicles. Two wires in the taillight jumper harness may be reversed, causing the turn signal to activate in the opposite direction of what the driver intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment."

NHTSAMar 7, 2024Nationwide• INTERNATIONAL

TRP Red Eye Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

International LT (International) – Steering Gear Shaft Issue (2024)

Navistar, Inc. (Navistar) is recalling certain 2025 International HV, HX, LT, and MV vehicles. The steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

NHTSAFeb 29, 2024Nationwide• INTERNATIONAL

TRP Aging Eye Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Eye Strain Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Blur Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

Pink Eye Relief Eye Drops (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Dryness Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Natural Eyes Floaters Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Allergy Eyes Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

TRP Eye Twitching Relief (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

HylaTears Lubricant Eye Drops (Optikem) – sterility risk (2024)

Lack of Assurance of Sterility

Class IIModerate

FDAFeb 29, 2024Nationwide• Optikem International, Inc.

QuickFlash Artery Catheterization (Arrow) – Component Defect (2024)

Teleflex is initiating this voluntary recall for the above-mentioned products due to reports received indicating a potentially defective component. The complaints received relate to resistance of the guidewire handle/chamber during use. The possible immediate health consequences of the component issue are arterial vasospasm and vessel injury arising from multiple arterial punctures with repeated attempts.

FDAFeb 12, 2024Nationwide• ARROW INTERNATIONAL Inc.

Jalapenos (M-C McLane International) – Glass Contamination (2024)

Glass contamination

Class IIModerate

FDAFeb 10, 2024AL, AZ, CA +25 more• M-C McLANE INTERNATIONAL