Phillips Bicycles Serial Numbers

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Made in Phillips Factory in Birmingham, England, in 1939. Frame serial number F34484. Typical to women’s bicycles of English origin, its frame has straight down tube. Bicycles & Framesets Bicycles & Frames is the newest collection to be added to VeloBase.com, and aims to collect information on the vast number of vintage bicycles in hopes of preserving information on both their original specifications as well as representing how cyclists ride them today.

Since used-bikes typically sell below their asking price, our analysis tracks actual sale prices to determine Private Party Value. Real-time Algorithm Our algorithm considers a bike's age, brand, type, frame material, suspension, condition, components, wheel size, modifications, manufacturer and retailer discounting and the depreciation that.
Vintage Bicycle Serial Numbers. Part of the series: Vintage Bicycles Styles. Bicycle serial numbers can be hard to locate and decipher. Learn how to read a v.

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Class 2 Device Recall Philips HeartStart (HS1) (Onsite/Home) AED

Z-1914-2018
Date Initiated by Firm	March 14, 2018
Create Date	May 23, 2018
Recall Status¹	Terminated ³ on August 19, 2020
Recall Event ID	79343
K020715
Automated external defibrillators (non-wearable) - Product CodeMKJ
Product	Philips HeartStart (HS1) Onsite/Home AED
Code Information	Manufactured between September 2002 and February 2013. The year of manufacture can be identified by the 2nd and 3rd characters in the serial number on the back of the AED in the following ranges: Home/Onsite: A02x-xxxxx through A13B-xxxxx; FRx: B04x-xxxxx through B13B-xxxxx NOTE: If the device was manufactured in 2013 and the 4th digit is the letter 'C' or later (D, E, F...), it is not covered by the recall (i.e. A13G-02375). In some cases, a device within the date range covered by the notification did not contain a resistor previously associated with a failure. In that case, a notification was not sent. Confirmation as to whether the device contains the resistor at issue can be done by contacting the firm.
Recalling Firm/ Manufacturer	Philips Electronics North America Corp. 22100 Bothell Everett Hwy Bothell WA 98021-8431
For Additional Information Contact	800-263-3342
An issue with one of the electric components (a resistor) could result in the device not delivering a shock when needed.
Nonconforming Material/Component
Letters dated 2/16/2018 for U.S. customers were issued via certified mail on 3/14/2018. Letters to customers outside of the U.S. were localized in conjunction with the local Philips market organizations and are in progress.
Total for FRx and HS1 - 660,519 defibrillators
Distribution was nationwide and to Puerto Rico. There was also government/military distribution. Foreign distribution was made to the following countries: Canada, Afghanistan, Algeria, Argentina, Aruba, Australia, Austria, Bahrain, Bangladesh, Belgium, Bolivia, Botswana, Brazil, Brunei Darussalam, Cambodia, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Fiji, Finland, France, Georgia, Germany, Ghana, Greece, Guatemala, Hong Kong, Iceland, India, Indonesia, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Kenya, Republic of Korea, Kuwait, Latvia, Lebanon, Libya, Lithuania, Luxembourg, Macao, Malaysia, Malta, Mauritius, Mexico, Morocco, Namibia, Netherlands, Netherlands Antilles, New Caledonia, New Zealand, Niger, Norway, Oman, State of Palestine, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Sri Lanka, Suriname, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirate, United Kingdom, Uzbekistan, Venezuela, Viet Nam, Yemen, Zambia, and Zimbabwe.
TPLC Device Report
¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. ² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. ³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database	510(K)s with Product Code = MKJ and Original Applicant = PHILIPS MEDICAL SYSTEMS

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