{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "114352", "product_res_number": "Z-0629-2013", "event_date_initiated": "2012-12-18", "event_date_posted": "2013-01-03", "recall_status": "Terminated", "event_date_terminated": "2013-08-30", "res_event_number": "63602", "product_code": "FNL", "product_description": "Medical Surgical Bed, Model 3005S3EX\n\nMedical Surgical Bed The S3\" MedSurg Bed, Model 3005 is intended to support and transport patients within the Med/Surg and Critical Care hospital environments. The bed is typically used in pre-op, post-op and recovery areas of hospital facilities. The intended user for this product is both Health Care Providers (HCPs: nurses, nurses aides, and medical doctors) and human patients. Lockout features may limit patient accessible controls.", "code_info": "Model 3005S3EX, Serial Number 120415087 - 120515468,", "firm_fei_number": "1831750", "recalling_firm": "Stryker Medical Division of Stryker Corporation", "address_1": "3800 East Centre Ave.", "city": "Portage", "state": "MI", "postal_code": "49002", "additional_info_contact": "Blaine Burnette\n269-488-8691", "reason_for_recall": "Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March 15, 2012 and May 23, 2012. may have been built with brake rings that do not meet specifications, negatively impacting the holding force of the brakes.", "root_cause_description": "Process control", "action": "Stryker sent an Urgent Medical Device Correction letterdated December 18, 2012, to all affected customer. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to locate the affected product and ensure that the brakes are holding properly. Consignees were directed to contact Stryker (1-800-327-0770, option 2) to make arrangements to replace all brake rings and continue to routinely inspect brake functionality. Customers were asked to Fax (269-488-8691) the enclosed acknowledgment and Stryker field service will contact customers to schedule service. Consignees were directed to forward a \ncopy of this notice to the new users and advise us of their new location.\nFor questions regarding this recall call 269-488-8691.", "product_quantity": "1004", "distribution_pattern": "Worldwide Distribution - Nationwide and Canada", "openfda": { "k_number": [ "K946149", "K962250", "K872923", "K964515", "K931482", "K962942", "K830559", "K982783", "K962763", "K963622", "K202964", "K894296", "K951161", "K963589", "K915437", "K881965", "K881963", "K821185", "K854832", "K951514", "K883463", "K854937", "K932663", "K853270", "K872924", "K926435", "K971546", "K854867", "K935837", "K873291", "K872925", "K946208", "K931581", "K831821", "K890845", "K922352", "K963701", "K972115", "K890426", "K790049", "K974254", "K930703", "K900151", "K902183", "K851551", "K843781", "K934090", "K974296", "K964246", "K811897", "K864172", "K875037", "K945664", "K951735", "K930234", "K903904", "K925576", "K103536", "K881782", "K893745", "K890293", "K911893", "K881027", 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