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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 261–280 of 1146 recalls

ARROW INTERNATIONAL Inc.: Arrow MAC Two-Lumen Central Venous Access Kit fr use with...

There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.

FDAOct 27, 2022FL, GA, IN +4 more• ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc.: Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC ...

FDAOct 27, 2022FL, GA, IN +4 more• ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc.: Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow Auto...

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

1...12 131415 16...58

Page 14 of 58Next

FDA

Oct 17, 2022

Nationwide

• ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc.: Arrow AutoCAT 2 Intra-Aortic Balloon Pump, Arrow AutoCAT...

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

FDAOct 17, 2022Nationwide• ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc.: Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus...

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

FDAOct 17, 2022Nationwide• ARROW INTERNATIONAL Inc.

ARROW INTERNATIONAL Inc.: Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT 2 IAPB,...

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

FDAOct 17, 2022Nationwide• ARROW INTERNATIONAL Inc.

BluCrab Pasteurized Crabmeat (River City Seafood) – defective seal (2022)

Defective seal in cans containing pasteurized crabmeat.

Class IIModerate

FDAOct 14, 2022Nationwide• RIVER CITY SEAFOOD INTERNATIONAL LLC

Walgreens Sinus Medicine (LNK International) – Mislabeled Ingredients (2022)

Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg

Class IIILow

FDAOct 11, 2022Nationwide• LNK International, Inc.

Beaver Visitec International, Inc.: Beaver Arthro-Lok Pointed Tip Curve L 4mm Blade-an orthop...

Incorrect configuration of the blades in the package. The blades curve to the right instead of curving to the left. If used may cause cause unintended tissue damage during the procedure or if noticed prior to use may cause a delay in surgery

FDASep 30, 2022FL, GA, IN +4 more• Beaver Visitec International, Inc.

2022 INTERNATIONAL HX Recall: STEERING:LINKAGES:TIE ROD ASSEMBLY

Navistar, Inc. (Navistar) is recalling certain 2022-2023 International HX vehicles. The tie rod clamps may have been improperly heat-treated, causing them to fail and allowing the tie rods to separate.

NHTSASep 22, 2022Nationwide• INTERNATIONAL

International Medical Industries, Inc.: Prep-Fill Guarded Luer Connector (GLC): a. Part Number...

Blister package had an unsealed edge compromising sterility.

FDASep 16, 2022Nationwide• International Medical Industries, Inc.

2018 INTERNATIONAL LT Recall: ENGINE

Navistar, Inc. (Navistar) is recalling certain 2018-2021 International HV, 2018-2020 International HX, 2018-2021 International LT and International RH vehicles. The connecting rod wrist pin may crack, resulting in connecting rod failure.

NHTSASep 15, 2022Nationwide• INTERNATIONAL

Sanitizing Hand Spray (Salon Technologies) – Chemical Contamination (2022)

GMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.

Class IIModerate

FDASep 14, 2022FL, WA• Salon Technologies International Inc

ARROW INTERNATIONAL Inc.: ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lum...

Mislabeling: the corrugate label, lidstock, banner card, and peel sticker accompanying the affected product incorrectly displays a double lumen 5.5 French catheter (and related priming volumes and kit contents for product code ASK-41552-JHVA1), instead of the packaged single-lumen 4.5 French catheter (and related priming volumes and kit contents for product code ASK-41541-JHVA1).

FDASep 14, 2022Nationwide• ARROW INTERNATIONAL Inc.

Antica Farmacista Hand Sanitizer (Salon Technologies) – Benzene Risk (2022)

Chemical Contamination: product found to contain benzene

Class IHigh

FDASep 14, 2022FL, WA• Salon Technologies International Inc

2023 INTERNATIONAL MV Recall: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM)

Navistar, Inc. (Navistar) is recalling certain 2023 International LT, International Lonestar, International MV, International HV, International HX, and IC Bus TC Commercial buses. The engine control module (ECM) may experience an internal electrical short-circuit, causing the engine to stall.

NHTSAAug 10, 2022Nationwide• INTERNATIONAL

Nighttime Sleep-Aid (LNK International) – Incorrect Labeling (2022)

Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.

Class IIILow

FDAAug 4, 2022Nationwide• LNK International, Inc.

Underwater Communication Devices (Ocean Technology) – fire hazard (2022)

Fire/Burn Risk

This recall involves the PowerCom 3000D, 5000D and MilCom 6000D underwater communication devices sold with the RBLi-4 Lithium battery pack and the batteries that are also sold separately. The PowerCom, MilCom and RBLi-4 products are used in all SCUBA diving. The recalled RBLi-4 battery packs are in a waterproof housing and supply power to the PowerCom and MilCom products. PowerCom and MilCom along with the model numbers are printed on the front of the underwater communication devices.

CPSCJul 28, 2022Nationwide• Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California

2016 INTERNATIONAL LT Recall: ELECTRICAL SYSTEM:12V/24V/48V BATTERY:CABLES

Navistar, Inc. (Navistar) is recalling certain 2018-2021 International LoneStar and 2016-2021 International LT vehicles. The cables that connect the batteries to the vehicle frame may become excessively hot, and in some cases, cause battery post separation.

NHTSAJul 28, 2022Nationwide• INTERNATIONAL

LiftActiv Peptide-C Ampoules (Vichy Laboratoires) – Laceration Risk (2022)

Laceration Risk

This recall involves Liftactiv Peptide-C Ampoules 1.8ml (10 pack) and Liftactiv Peptide-C Ampoules 1.8ml (30 pack) which are facial serums. The serum is packaged in amber-colored glass ampoules with the following batch numbers: 54T61Q, 54T91Q, 54TD1Q, 54TD2Q, 54TN1Q, 54TN2Q, 54TN3Q, 54TO1Q, 54U11Q, 54U12Q, 54U21Q, 54U31Q, 54U32Q, 54U41S, 54U42S, 54U51S, 54U52S, 54U53S, 54U54S, 54U61S, 54U72S, 54U91S, 54U62S, 54U92S, 54UD1S, 54UO1S, 54W11S, 54W12S, 54W13S, 54W21S. The batch number is printed on the bottom or side of the pack.

CPSCJul 21, 2022Nationwide• Cosmetique Active Internationale, of France