{ "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": "2026-08-13", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "176297", "product_res_number": "Z-0107-2020", "event_date_initiated": "2019-04-24", "event_date_created": "2019-10-09", "recall_status": "Terminated", "event_date_terminated": "2020-04-03", "res_event_number": "83584", "product_code": "LRP", "k_numbers": [ "K171957" ], "product_description": "UVC TRAY\nUVT875", "code_info": "2017051690 2017052390 2017071390 2017072490 2017082490 2017090790 2017100490 2018012590 2018062890 2018071290 2018081990 2018101290", "firm_fei_number": "3008403546", "recalling_firm": "Centurion Medical Products Corporation", "address_1": "100 Centurion Way", "city": "Williamston", "state": "MI", "postal_code": "48895-9086", "additional_info_contact": "Lisa A. Carpenter\n517-546-3356", "reason_for_recall": "Firm distributes kits which include the BD MaxZeroNeedleess Connector, which was recalled by the manufacturer due to the potential for droplets of fluid separating from the sealed surface of the connector following disconnection.", "root_cause_description": "Under Investigation by firm", "action": "On April 24, 2019, the firm notified customers who had received kits containing BD's MaxZero product. \n\nCustomers were instructed to do the following:\n\n1. Whether or not you have product in inventory, please complete and return the\nattached Centurion Accountability Record via email- lcarpenter@centurionmp.com or\nvia fax-517-546-3356. \n2. Please share this communication with all users of the product within your\norganization, as directed in the BD letter.\n3. Report any adverse health consequences experienced with the use of this product to\nBD. Events may also be reported to the FDA's MedWatch Adverse Event Reporting\nprogram.\nWeb: MedWatch website at www.fda.gov/medwatch Phone: 1-800-FDA-1088 (1-\n800-332-1088); Mail: MedWatch, HF-2, FDA, 5600 Fisher's Lane, Rockville, MD 20852-\n9787", "product_quantity": "181965 total", "distribution_pattern": "Nationwide domestic distribution.", "openfda": { "k_number": [ "K903544", "K883098", "K940646", "K905462", "K873439", "K922126", "K873290", "K903962", "K890071", "K903963", "K912105", "K881095", "K760497", "K882275", "K874665", "K873469", "K963723", "K940444", "K951811", "K935621", "K861142", "K940239" ], "registration_number": [ "3009340886", "3014644369", "3005625540", "3007773213", "8040881", "3003120897", "2084725", "3001650535", "3007539489", "1421879", "3018094310", "2242056", "9611062", "3032747418", "3014908171", "1000124971", "3017410889", "1037577", "3031240334", "3009158523", "3016171961", "1450662", "3015168527", "3007420745", "3010757045", "3044150131", "1054241", 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