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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

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 5481–5500 of 37665 recalls

Arrow ErgoPack (Arrow) – Product Label Mismatch (2023)

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

Moderate

FDAAug 10, 2023Nationwide• ARROW INTERNATIONAL Inc.

Welch Allyn Connex Monitor (Baxter) – Display Tape Placement (2023)

Product is being recalled due to the improper placement of a copper tape on the back of the liquid-crystal display.

Moderate

FDAAug 10, 2023Nationwide• Baxter Healthcare Corporation

Room & Board Crib Mattresses (Restwell) – suffocation hazard (2023)

This recall involves Room & Board brand crib mattresses, Natural Organic Latex and Spring Crib (Model no. 847564) and Natural Organic Latex Crib (Model No. 925869). The crib mattresses are 52 inches long and 28 inches wide, have a white top and gray sides with "Room & Board" embroidered on one end with the model name underneath.

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Very High

CPSCAug 10, 2023Nationwide• Restwell Mattress Co., of Eden Prairie, Minnesota

Arrow ErgoPack PICC (Arrow) – Product Label Mismatch (2023)

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

Moderate

FDAAug 10, 2023Nationwide• ARROW INTERNATIONAL Inc.

Hello Strawberry Toothpaste (Colgate) – labeling issue (2023)

Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as hello fresh watermelon fluoride free toothpaste.

Class IIModerate

FDAAug 10, 2023Nationwide• Colgate Palmolive Company

Toll House Cookie Dough (Nestle) – wood fragment risk (2023)

Potential presence of wood fragments.

Class IIModerate

FDAAug 10, 2023AL, AZ, CA +25 more• Nestle-USA, Inc. (Corporate Office)

Oculus Pentacam AXL Wave (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Oculus Myopia Master (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

Prucka 3 Amplifiers (GE Medical) – Power Supply Failure (2023)

A diode on the power supply of the Prucka 3 Amplifier used with CardioLab/ComboLab systems could reach elevated temperatures and fail, then power off and become inoperable.

Moderate

FDAAug 8, 2023CA, CO, FL +14 more• GE Medical Systems Information Technologies Inc

Oculus Pentacam AXL (Oculus) – Coating Measurement Risk (2023)

Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.

Moderate

FDAAug 8, 2023Nationwide• Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany

ADVIA Chemistry Iron Reagents (Siemens) – QC Result Bias (2023)

There is a potential for a positive bias on Quality Control (QC) and patient sample results when using some IRON_2 reagent wedge pairs. When the issue occurs, the observed bias will vary wedge to wedge.

Moderate

FDAAug 8, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Heartmate 3 LVAS Kit (Thoratec) – Coring Knife Sharpness (2023)

Inability to start and/or complete the coring procedure due to inadequate sharpness of the Apical Coring Knife, provided with Left Ventricular Assist System, could result in an extended procedure or surgical time while the backup coring knife is acquired.

Moderate

FDAAug 7, 2023Nationwide• Thoratec Corp.

Forest River Sierra (Forest River) – Axle Installation Error (2023)

Forest River, Inc. (Forest River) is recalling certain 2024 Sandpiper, and Sierra fifth wheels. The axle may be installed backwards, which can reduce braking ability.

Moderate

NHTSAAug 7, 2023Nationwide• FOREST RIVER

Stryker ACM Cement Mixing System (Stryker) – Nozzle Breakage Risk (2023)

Potential for the Break-Away Femoral Nozzle the applicator tip connecting the cement cartridge, to disassemble or break off during use, can lead to the potential for loss of function of the ACM system and bio-incompatibility due to components falling into surgical site

Moderate

FDAAug 7, 2023Nationwide• Stryker Corporation

Forest River Pause (Forest River) – Awning Security (2023)

Forest River, Inc. (Forest River) is recalling certain 2023 Forest River Pause travel trailers. The awning may not be adequately secured, which can cause the awning to detach.

Moderate

NHTSAAug 7, 2023Nationwide• FOREST RIVER

Hudson RCI Addipak (Medline) – Sterility Failure (2023)

Product dispositioned for scrap for sterility failure investigation that was inadvertently shipped to customers.

Moderate

FDAAug 4, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield

Amana PTAC Air Conditioners (Daikin) – Potential module issue (2023)

Fire/Burn Risk

This recall involves Amana-branded Packaged Terminal Air Conditioners and Heat Pumps (PTACs) assembled with "DigiAir" modules. DigiAir modules are factory-installed make-up air systems with configurable dehumidification. The recalled units are beige and have a model number that begins with PMH or PMC. Amana is printed on the unit's control cover and the model number is on the label located below the control board.

High

CPSCAug 3, 2023Nationwide• Daikin Comfort Technologies Manufacturing L.P. (DCT), of Houston, Texas

Avent Baby Monitors (Philips) – Burn risk (2023)

Fire/Burn Risk

This recall involves Philips Avent video baby monitors used to remotely monitor infants. They consist of a Baby Unit (camera) and a Parent Unit (monitor) pair. The monitor has a 3.5-inch color screen. The recalled baby monitors include models SCD630 and SCD843 only, manufactured between March 2016 and December 2019. The model numbers and production date codes, in day-month-year format, are located on the bottom of the Parent Unit. The monitors and camera are white. Philips Avent is printed on the front.

High

CPSCAug 3, 2023Nationwide• Philips Consumer Lifestyle B.V., of The Netherlands

Upper Roller Bracket (Accuray) – service clearance problem (2023)

It is possible the upper roller bracket in the Radixact System gantry enclosure may not provide enough clearance for service personnel to use a jib crane for moving components while servicing the system, resulting in possible injury to the service personnel.

Moderate

FDAAug 3, 2023Nationwide• Accuray Incorporated

ReNewal Ligasure Sealer (MEDLINE) – packaging seal issue (2023)

Various reprocessed Covidien LigaSure and Ethicon Harmonic devices may have an incomplete seal on the packaging tray.

Low

FDAAug 3, 2023Nationwide• MEDLINE INDUSTRIES, LP Northfield