{ "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": "2026-08-27", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "131363", "product_res_number": "Z-0559-2015", "event_date_initiated": "2014-09-08", "event_date_posted": "2014-12-16", "recall_status": "Terminated", "event_date_terminated": "2017-11-29", "res_event_number": "69471", "product_code": "HKY", "product_description": "Schoitz weights are manual devices used with Schoitz tonometers and are intended to measure intraocular pressure by applying a known force on the globe of the eye and measuring the amount of indentation produced (Schiotz type) or to measure intraocular tension by applanation (applying a small flat disk to the cornea) and are sold under the Ambler Surgical brand name.", "code_info": "1) Instrumed Product Name: Schoitz Weights 7.5 grams; Instrumed Product Number: 720-55812; Trade Name: Ambler Surgical; Ambler Surgical Product Name: Schoitz Weights 7.5 grams; Ambler Surgical Item Number: 5754B; Lot Number: 050411.   2) Instrumed Product Name: Schoitz Weights 15.0 grams; Instrumed Product Number: 720-55822; Trade Name: Ambler Surgical; Ambler Surgical Product Name: Schoitz Weights 15.0 grams; Ambler Surgical Item Number: 5754F; Lot Number: 050411.", "firm_fei_number": "1421101", "recalling_firm": "Instrumed International, Inc.", "address_1": "626 Cooper Ct", "city": "Schaumburg", "state": "IL", "postal_code": "60173-4537", "additional_info_contact": "Ms. Jennifer S. Staunton\n847-908-6119", "reason_for_recall": "The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet all FDA requirements to market the devices as \"Pre-Amendment\" devices.", "root_cause_description": "No Marketing Application", "action": "Instrumed sent an URGENT: MEDICAL DEVICE MARKET WITHDRAWAL letters dated October 9, 2014 to all affected customers. The letter included instructions for customers to: 1) examine their inventory to determine if there are any recalled devices; 2) complete and return the enclosed Confirmation Request Form; 3) return the recalled devices; and 4) share the recall information with facility staff. Customers with questions were instructed to contact Instrumed by telephone at 847-908-6119.", "product_quantity": "3 Schoitz weights", "distribution_pattern": "Nationwide Distribution including AZ, CA, FL, IL, KS, MI, NC, OH, PA, TN, TX, and VA.", "openfda": { "k_number": [ "K142179", "K070534", "K924760", "K781105", "K945446", "K234037", "K220852", "K151491", "K132917", "K172728", "K241447", "K923877", "K071755", "K992998", "K964312", "K032967", "K133234", "K203850", "K132549", "K152644", "K093445", "K945541", "K142263", "K813619", "K981432", "K834187", "K063873", "K772130", "K211355", "K000288", "K153694", "K032769", "K152308", "K832996", "K023838", "K232143", "K163343", "K970887", "K011199", "K233516", "K882750", "K992835", "K200966", "K180839", "K991840", "K033146", "K173904", "K960924", "K053430", "K860330", "K961512", "K852774", "K182491", "K190316", "K191314", "K022054" ], "registration_number": [ "1225798", "3005528784", "1000176188", "1721676", "3038356864", "2080939", "9616517", "3006550126", "3010610157", "3005324856", "1226586", "3009173773", "3011223751", "3004095901", "3010399798", "3002894792", "9611112", "9710516", "3005809810", "3012375451", "3010383847", "3019907057", "2431166", "3004441848", "2031962", "3009756153", "3008770252", "3009576895", "3005906810", "3011898560", "3004950803", "3010155661", "1313525", "2245304", "1526534", "1319721", "1932180", "3007744213", "3008132398", "3010287677", "3015177648", "3003617485", "9616199", "2219920", "3005755367", "1527493", "3012302888", "3005785090", "2245590", "3010227033", "3015895045", "1000391004", "3004215117", "8010482", "3004681519", "3009496855", "2521877", "8020986", "3015972897", "3014865", "2242450", "3003418325", "1836161", "8044131" ], "fei_number": [ "3005528784", "2523865", "1000176188", "3002807091", "1721676", "3038356864", "4196", "1000119305", "2080939", "3006550126", "3010610157", "3001802794", "3005324856", "3009173773", "3011223751", "3004095901", "3010399798", "3002894792", "3005809810", "3012375451", "3010383847", "3019907057", "3004441848", "3009756153", "3008770252", "3009576895", "3005906810", "3011898560", "3003870583", "3004950803", "1000292048", "3010155661", "2245304", "1526534", "3007744213", "3010287677", "3015177648", "3001595430", "3003617485", "2219920", "3005755367", "3004545399", "1527493", "3012302888", "3008782585", "3005785090", "2245590", "3010227033", "3015895045", "1317628", "1000391004", "3004215117", "2521877", "3009496855", "1000159913", "3003117688", "3003156974", "3015972897", "3014865", "3003768492", "2242450", "3003418325", "3002445546", "3002750084" ], "device_name": "Tonometer, Manual", "medical_specialty_description": "Ophthalmic", "regulation_number": "886.1930", "device_class": "2" } } ] }