{ "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": "2026-09-17", "results": { "skip": 0, "limit": 1, "total": 5 } }, "results": [ { "cfres_id": "188981", "product_res_number": "Z-2597-2021", "event_date_initiated": "2021-08-11", "event_date_created": "2021-09-30", "recall_status": "Open, Classified", "res_event_number": "88548", "product_code": "FSA", "product_description": "OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient.\nModel Number: 3156056", "code_info": "N/A", "firm_fei_number": "1824206", "recalling_firm": "Hill-Rom, Inc.", "address_1": "1069 State Road 46 E", "city": "Batesville", "state": "IN", "postal_code": "47006-7520", "additional_info_contact": "Howard Karesh Chicago, Illinois 312 \n312-237-6188", "reason_for_recall": "Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.", "root_cause_description": "Under Investigation by firm", "action": "Hillrom issued URGENT Medical Device Correction letter dated August 11, 2021 by third party vendor via UPS mail/track the delivery to consignees. Letter states reason for recall, health risk and action to take: \nHillrom is initiating this Medical Device Correction to all customers and will be correcting devices with an updated to the leveller.\nActions being taken by Customer:\nPlease share this Medical Device Correction with all potential users in your organization. Please ensure inspection of the device prior to use as stated in the device Instruction for Use (IFU). Complete the attached response form, acknowledging receipt, indicate the number of devices and return to hillromLUL003@stericycle.com within one month", "product_quantity": "440 units", "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, DE, IL, \nME, MI, MO, MS, NJ, OH, PA, VA, WA and the countries of Argentina, Australia, Austria, \nBolivia, Canada, China, Colombia, Costa Rica, Croatia, Czech Republic, Denmark, Finland, France, Germany, Great Britain, Greece, Hong Kong, India, Ireland, Italy, Japan, \nJordan, Kuwait, Latvia, Lithuania, Mexico, Netherlands, Norway, Poland, Portugal, \nSerbia, Slovakia, Spain, Sweden, Switzerland, Taiwan, Province of China, Thailand, \nTurkey, United Arab Emirates.", "openfda": { "k_number": [ "K841395", "K841398", "K930625", "K844976", "K860837", "K840997", "K942807", "K780684", "K902141", "K823206", "K792601", "K811899", "K851844" ], "registration_number": [ "3009709183", "3013875443", "2183887", 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