2024 Product Recalls

Side Marker Lights Not Reflective/FMVSS 108

Non-reflective side marker lights can reduce the trailer's visibility to other drivers, increasing the risk of a crash.

Dealers will replace the marker lights, free of charge. Owner notification letters were mailed January 24, 2024. Owners may contact Forest River Customer Service at 1-574-821-1311. Forest River's number for this recall is 53-1724.

Independent Suspension May Detach

A detached independent suspension can increase the risk of a crash.

Dealers will inspect the fasteners and replace or secure them as necessary, free of charge. Owner notification letters were mailed February 20, 2024. Owners may contact Forest River Customer Service at 1-574-642-1612. Forest River's number for this recall is 51-1727.

Overloaded Electrical System May Cause Fire

Overloaded electrical circuits can overheat, increasing the risk of fire.

Maron will work with the equipment manufacturer Weldon to update the firmware, free of charge. Owner notification letters were mailed January 26, 2024. Owners may contact Marion Body Works customer service at 1-715-754-5261.

High Voltage Cables Labeled Incorrectly

A mislabeled electrical cable may be mistaken for a de-energized cable by a technician or first responder, increasing the risk of electrical shock and injury.

Dealers will inspect the high voltage cables and add white high voltage tape as necessary, free of charge. Owner notification letters were mailed February 05, 2024. Owners may contact Navistar customer service at 1-800-448-7825. Navistar's number for this recall is 24502.

Driver's Seat Belt Bolt Not Properly Attached

An improperly anchored seat belt tether may not restrain an occupant as intended, increasing their risk of injury during a crash.

Dealers will inspect and replace the seat belts as necessary, free of charge. Owner notification letters were mailed February 26, 2024. Owners may contact Navistar customer service at 1-800-448-7825. Navistar's number for this recall is 24501.

Roof Molding May Detach

A detached roof molding can create a road hazard for other vehicles, increasing the risk of a crash.

Dealers will inspect the roof molding and replace or secure it as necessary, free of charge. Owner notification letters were mailed March 15, 2024. Owners may contact Kia customer service at 1-800-333-4542. Kia's number for this recall is SC292.

Blind Spot Monitoring System May Fail

Without a functioning blind spot monitoring system, the driver may be unaware of a vehicle in their blind spot, which can increase the risk of a crash.

Dealers will install a new blind spot monitoring system, free of charge. Owner notification letters are expected to be mailed February 16, 2024. Owners may contact Winnebago customer service at 1-641-585-6939 or 1-800-537-1885.

Rearview Camera Image May Not Display/FMVSS 111

A rearview camera image that does not display while in reverse decreases the driver's visibility, increasing the risk of injury or crash.

Dealers will inspect the rearview camera and add a new seal or replace the camera, free of charge. Owner notification letters were mailed to Range Rover owners March 4, 2024. Interim notification letters were mailed to Range Rover Sport owners March 7, 2024. Range Rover Sport owners will receive a second notice once remedy parts become available. Owners may contact Land Rover customer service at 1-800-637-6837. Land Rover's number for this recall is N778.

ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media.

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).

The firm sent an URGENT MEDICAL DEVICE NOTFICATION to its sole consignee on 09/15/2022, by FedEx 2-day mail. The letter explained the reason for recall and requested the following: "Please adhere to the following actions: 1. Check your inventory for products in scope of this advisory notice. 2. If you do not have affected product, mark the applicable checkbox on the Acknowledgement Form (Appendix 2) and return the form to Teleflex Customer Service using the contact information below. 3. If you have affected product, mark the applicable checkbox on the Acknowledgement Form (Appendix 2), return the form to Teleflex Customer Service using the contact information below, and place a copy of this advisory notice with all affected products. Adverse reactions or quality problems experienced with the use of this product should be reported to Teleflex Customer Service using the contact information below or may also be reported to the FDA s MedWatch Adverse Event Reporting program either by phone at 1-888-INFO-FDA (1-888-463-6332) or online at https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverseevent-reporting-program. Transmission of this Advisory Notice This advisory notice should be passed on to all persons who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. Please consider end users, clinicians, risk managers, supply chain/distribution centres, etc., in the circulation of this notice. Please maintain awareness of this notice until all required actions have been completed in your organization.

BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10

When updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.

A MEDICAL DEVICE CORRECTION notification letter dated 3/9/22 was distributed to customers. PLEASE TAKE THE FOLLOWING ACTIONS: 1. Ensure the contents of this notification are read and understood by those within your organization. 2. BD will be contacting you within one week to request remote access to your database to confirm your configuration and evaluate potential impact. If BD determines that your facility has an affected configuration, BD will work with your facility to resolve the issue. In the interim, you many continue use of the product until BD contacts your facility. 3. Complete the attached Customer Response Form and return to the BD contact noted on the form so that BD may acknowledge your receipt of this notification per FDA requirements. 4. Report any adverse health consequences experienced with the use of this product to BD. Events may also be reported to the FDA's MedWatch Adverse Event Reporting program via: Web: MedWatch website at www.fda.gov/medwatch Phone: 1-800-FDA-1088 (1-800-332-1088) Mail: MedWatch, HF-2, FDA, 5600 Fisher s Lane, Rockville, MD 20852-9787 Actions Taken by BD: 1. BD will review configuration and evaluate potential impact for BD Kiestra customers. 2. Corrective actions have been initiated to prevent recurrence of the identified root cause. If you require further assistance, please contact:

MedMinder Medication Dispenser- Intended to serve as a medication reminder to promote medication adherence with additional feature to communicate with emergency call center.

Discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feature(button) removed

Medminder engaged a third-party vendor to perform the phone calls and notifications. The process was initiated on 03/28/2022. Initial contact via telephone and text message. Formal letter issued first week of April 2022, formal certified letters to all relevant customers notifying them of the removal of the pendant/watch and that it will no longer be supported (will no longer connect to the emergency alert system). . As of this notification, the medical alert pendants and watches will not work when pressed to call for emergency services. Please put in trash. Customers can still use the medical alert feature with the pill dispenser itself or call 911 or any other emergency system available to them. Older models (412 units) without the screen, the medical alert feature using the mechanical button has been removed and should not be relied on and there is no support for the red emergency alert button on your model of the MedMinder pill dispenser, and should not be used to contact emergency services. Please know that you should call 911 in the event of an emergency. If you were scheduled in the past for replacement of the pill dispenser with a newer model, it will be completed as scheduled. Notification letters were issued depending on the model being used by the customers as follows: 1. Letter to newer models regarding the accessory pendant only. 2. Letter to older models regarding the accessory pendant as well as the feature. 3. Introductory letter for subgroup of 29 customer with both older and newer models.

10 ga ARS Decompression Needle, Part Number ZZ-0298

The device includes the incorrect Instructions for Use.

Consignees will be notified by 09/01/2021 via email with read/delivery receipt followed by First Class Mail letter. Additionally, the recall notification will be posted to the firm's website, www.marescue.com. Consignees are asked to do the following: 1. Examine your inventory and quarantine all product identified in this recall notification. 2. Discontinue all distribution or use of the recalled products identified in this recall notification. 3. Identify the ZZ-0298, with the aid of ENCLOSURE 1, and verify the recalled lot W668NI, W693WF, W694ZH, W695DD, W696FN, or W697IJ. UDI number 00842209108831. 4. Complete the Recall Return Response Form in ENCLOSURE 2, including all requested information, even if you do not have the recalled product. 5. Contact recalls@narescue.com and provide your completed Recall Return Response Form in order to receive a replacement and arrange for the return of the recalled lots. 6. For assistance completing these steps or questions regarding your order, please contact NAR Customer Service toll free at 1-888-689-6277. (Please have your customer order number available to reference.) This recall should be carried out to the user level. Your assistance is appreciated and necessary to prevent patient harm. If you have further distributed this product, please: 1. Identify your customers and immediately notify them of this product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. Please complete and return the Recall Return Response Form, in ENCLOSURE 2, as soon as possible. If you have any questions, call William Slevin at (864) 675-9800.

Loss of Power Steering Assist

Loss of power steering assist while driving increases the risk of a crash.

Dealers will replace the spring engaging the worm gear and reapply grease to the gear teeth, free of charge. Owner notification letters were mailed March 6, 2024. Owners may contact Mazda customer service at 1-800-222-5500 Option 6. Mazda's number for this recall is 6524A.

Reversed Connections in ABS Computer/FMVSS 121

In the event of a wheel-lockup, the ABS computer may activate the air brakes on the opposite side of the trailer, reducing braking effectiveness and increasing the risk of a crash.

Dealers will correct the ABS computer connections, free of charge. Owner notification letters were mailed February 05, 2024. Owners may contact Lode-King customer service at 1-204-325-4345 or 1-866-797-0669 (toll free).

Brake Pedal Box Housing Improperly Welded

Reduced braking performance or a total loss of braking ability can increase the risk of a crash.

Dealers will replace the pedal box assembly, free of charge. Owner notification letters were mailed January 31, 2024. Owners may contact MMC customer service at 1-749-656-2632. MMC's number for this recall is MMC2023-001.