RecoveryAir Prime Advanced compression simplified for everybody. Your RecoveryAir Prime pneumatic compression system comes with a pump, a set of compression boots, two blocker plugs, a DC power adapter, and a carrying pouch. See Warnings on pg. 10 for important safety instructions.
Getting started 1. To turn on the RecoveryAir Prime pump, press and hold the power button. 2. To get started, put your boots on first before attaching them to the pump. This allows you to get into the most comfortable position and avoid any disruption in the air flow connection. 3. Next, plug in the connector from the boots into the pump. Make sure you hear a “click” so that you know the RecoveryAir Prime is fully connected, is plugged in, and there is a proper seal. 4.
Feature Callouts Buttons Indicators Power Button Warning Indicator Start/Pause/Stop Button Indicator lights up solid ON or blinking when a device malfunction is detected Time Button: Bluetooth Indicator 4 time intervals (20, 40, 60, and continuous) Indicator turns ON only when connected to the App Pressure UP/Down Button: Battery Indicator Adjustable Pressure Range (20-100 mmHg) in increments of 10 mmHg 3 LED lights to indicate battery life Adjustable pressure changes via the Therabody app in i
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RecoverAir Prime Programs About negative gradient for all programs: The RecoveryAir Prime’s unique true negative gradient of pressure sequentially travels up the limb from the foot toward the heart in four internal overlapping chambers. The spiraling overlap of chambers safely maximizes circulation. • The pressure can be the same in two consecutive chambers, but the pump won’t allow a back chamber to have a higher pressure than a front chamber. • The minimum pressure level of each chamber is 20 mmHg.
Chamber 4 Chamber 3 Chamber 2 Chamber 1 Figure 1 - Sequential Cycle Mode 6
Smart Features The RecoveryAir Prime also connects to the Therabody app via Bluetooth, giving you control of your RecoveryAir Prime session from the convenience of your smartphone. Not only can you easily access the Recover and Warm-up treatment options, but you can also adjust the pressure and time. Scan the QR code to get started.
Charging the RecoveryAir Prime 1. 2. 3. After turning off the pump, plug the power adapter into the charging port of the RecoveryAir Prime pump. You can continue to use the RecoveryAir Prime while charging. Charging is complete when all 3 LED lights of the LED battery indicator are lit. Traveling with your RecoveryAir Prime Compression System When traveling with your RecoveryAir Prime Compression System, we recommend: • Roll the hose tightly and slide it into the foot section of your garment.
Superior, hygienic design It’s important to take proper care of your RecoveryAir Prime compression boots because the longer they last, the longer you will feel the benefits. RecoveryAir Prime compression boots have non-porous medical grade material that help fight bacteria and provide a resistant surface. Our internal overlapping chambers provide a smooth surface to clean, this means no wiping under chamber flaps where bacteria can build up. This also means, no smells.
Important Safety Information Read all instructions before using the RecoveryAir Prime Compression System for the first time Warning • • • • This system is intended for use by people in good health. This system is not recommended for people who have heart problems, or vascular problems, have a condition requiring the use of any medical device, or have any condition that may affect their normal well-being. If you are, or may be, pregnant, consult with your physician before use.
Important Safety Information Caution • • • • • • • • • • • • • • • • • • • 11 Do not operate the RecoveryAir Prime Compression System while operating a vehicle. Do not store or transport the RecoveryAir Prime Compression System beyond the specified temperature, humidity, and atmospheric pressure range. Do not use the RecoveryAir Prime Compression System beyond the specified temperature range: 10 to 30°C (50 to 86°F).
Labels The following labels and symbols appear on the pump, garments and/or packaging. Label IP 21 Description Location Degree of protection against ingress of water On pump base Read instructions before use On pump base Read instructions before use (for China only) On pump base Class III equipment (only in the EU per IEC60335-2-32) Equipment relying on limitation of voltage to extra-low-voltage (ELV) values as provision for basic protection and with no provision for fault protection.
Label 13 Description Location Read instructions before use On garment label Level of protection type BF applied part On pump base Double insulation On DC power adapter Direct current On pump base Manufacturer's name and address On garment label and on pump base Date of Manufacture On pump base
Label Description Location Unique Device Identification (UDI) On pump base and package, and garment bag and package Separate collection for waste electrical and electronic equipment On pump base In accordance with Directive 2014/35/EU electrical equipment designed for use within certain voltage limits, and Directive 2014/30/ EU electromagnetic compatibility On pump Serial number of the console On console base Fragile, handle with care On package 14
Label 15 Description Location Keep dry On package and console base.
Label Description Location "ON" (power) On power switch "OFF" (power) On power switch Do not wash On garment tag Do not dry-clean On garment tag Do not tumble dry On garment tag Do not bleach On garment tag Do not iron On garment tag 16
Indications for Use RecoveryAir is indicated for the temporary relief of minor muscle aches and pains, and for the temporary increase in circulation to the treated areas in people who are in good health. RecoveryAir simulates kneading and stroking of tissues by using an inflatable garment. Note • The pump is “multi-voltage” and can be used for travel. • An appropriate socket adapter must be used in countries with incompatible wall outlets. • Use only RecoveryAir garments with the RecoveryAir pump.
Note Possible Cause Action One garment inflates but the second one does not. The second garment does not receive air. Examine its hoses for kinks, twists and folds. The pump stops working, the Status Indicator turns On in yellow. Hose is not connected properly to garment or pump, or prong plug is not inserted into unused air outlet. Examine and fasten all air connections. When treating only one limb, always plug the unused air outlet with the prong plug provided with the pump.
Reporting adverse events to FDA MedWatch is the Food and Drug Administration’s (FDA) program for reporting serious reactions, product quality problems, therapeutic inequivalence/failure, and product use errors with human medical products, including drugs, biologic products, medical devices, dietary supplements, infant formula, and cosmetics. If you think you or someone in your family has experienced a serious reaction to a medical product, you are encouraged to take the reporting form to your doctor.
1. Report Online at: www.accessdata.fda.gov/scripts/medwatch/index. cfm?action=reporting.home 2. Consumer Reporting Form FDA 3500B. Follow the instructions on the form to either fax or mail it in for submission. For help filling out the form, see MedWatchLearn. The form is available at: www.fda.gov/downloads/aboutFDA/reportsmanualsforms/forms/ ucm349464.pdf 3. Call FDA at 1-800-FDA-1088 to report by telephone. 4. Reporting Form FDA 3500 commonly used by health professionals.
FCC compliance statement This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
• Consult the dealer or an experienced radio/TV technician for help. ISED compliance statement This device contains licence-exempt transmitter(s)/receiver(s) that comply with Innovation, Science and Economic Development Canada’s licence-exempt RSS(s). Operation is subject to the following two conditions: (1) This device may not cause interference. (2) This device must accept any interference, including interference that may cause undesired operation of the device.
VG Born in Los Angeles, CA. Designed for everybody.