Class 2 Device Recall SolM Syringes with exchangeable needles

• Date Initiated by Firm: May 09, 2024
• Date Posted: September 06, 2024
• Recall Status: Open, Classified
• Recall Number: Z-3075-2024
• Recall Event ID: 94968
• Product Classification: Syringe, piston - Product Code FMF
• Product: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml Luer Lock Syringe w/Safety Needle 21G*1 1/2 (needle aside), Model No. 102115SN, UPC 818392019858; 2) SOL-CARE 10ml Luer Lock Syringe w/Safety Needle 22G*1 1/2 (needle aside), Model No. 102215SN, UPC 818392019865; 3) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 25G*1 (needle aside), Model No. 12510SN, UPC 818392018851; 4) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 25G*5/8 (needle aside), Model No. 12558SN, UPC 818392018950; 5) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 27G*1/2 (needle aside), Model No. 12705SN, UPC 818392018967; 6) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 30G*1/2 (needle aside), Model No. 13005SN, UPC 818392018974; 7) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 21G*1 (needle aside), Model No. 32110SN, UPC 818392019001; 8) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 21G*1 1/2 (needle aside), Model No. 32115SN, UPC 818392019018; 9) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 22G*1 (needle aside), Model No. 32210SN, UPC 818392019025; 10) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 22G*1 1/2 (needle aside), Model No. 32215SN, UPC 818392019032; 11) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 23G*1 (needle aside), Model No. 32310SN, UPC 818392019049; 12) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 25G*1 (needle aside), Model No. 32510SN, UPC 818392019063; 13) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 25G*5/8 (needle aside), Model
• Code Information: a) SOL-M: 1) Model No. 1812010, UPC 818392010268, Lot Numbers: 4202007; 2) Model No. 1812015, UPC 818392010275, Lot Numbers: 4110010; 3) Model No. 1812110, UPC 818392010244, Lot Numbers: 4202008; 4) Model No. 1812115, UPC 818392010251, Lot Numbers: 2108094, 4110087, 4110088, 4303013, 4303015, 4304027, 4311001, 4312014, 4312022; 5) Model No. 1812210, UPC 818392010237, Lot Numbers: 4302040; 6) Model No. 1832010, UPC 818392011586, Lot Numbers: 4110005; 7) Model No. 1832015, UPC 818392010114, Lot Numbers: 1010016, 1012011, 1012019, 1110067, 1112021, 1112056, 1301021, 4110005; 8) Model No. 1832110, UPC 818392010084, Lot Numbers: 5105119, 19041740; 9) Model No. 1832115, UPC 818392010091, Lot Numbers: 4106053, 4202035, 4306035; 10) Model No. 1832210, UPC 818392010039, Lot Numbers: 4110006, 4209012; 11) Model No. 1832215, UPC 818392010077, Lot Numbers: 4102053, 4106153, 4202003, 4202003, 4306034, 4307015, 4307043, 4308047, 4309030, 4309040, 4310033; 12) Model No. 1832310, UPC 818392010107, Lot Numbers: 4102058, 4102059, 4103020, 4103021, 4103028, 4103029, 4106048, 4106049, 4106052, 4110007, 4110053, 1902183, 19021824; 13) Model No. 1832510, UPC 818392010053, Lot Numbers: 4012001, 4102056, 4103014, 4103015, 4103022, 4103023, 4103030, 4103031, 4106050, 4106051, 4109091, 19021825, 19021826, 19041742; 14) Model No. 1832515, UPC 818392010046, Lot Numbers: 4012002, 4102054, 4103018, 4103019; 15) Model No. 1832558, UPC 818392010022, Lot Numbers: 4007045, 40 10033, 4102050, 4102051, 4102052, 4103016, 4103017, 4110011, 4110012; 16) Model No. 1852010, UPC 818392010190, Lot Numbers: EXPIRED 17) Model No. 1852015, UPC 818392010206, Lot Numbers: EXPIRED 18) Model No. 1852115, UPC 818392010183, Lot Numbers: 4103076, 4105110; 19) Model No. 1852215, UPC 818392010169, Lot Numbers: 4001001, 4003019, 4110083, 4110084, 4202004, 4308046, 4308088, 4312097, 19052010; 20) Model No. 110101120011, UPC 818392014341, Lot Numbers: 4212007, 4306027, 4308066, 19030602; 21) Model No. 110101120012, UPC 818392014358, Lot Numbers: 4001021, 4008151, 4104087, 4110036, 4202006, 19030603; 22) Model No. 1832110T, UPC 818392012880, Lot Numbers: 4103002, 4104043, 4105120, 4106152, 4109083, 4110045, 4111040, 4206041, 4206042, 4206043, 4208008, 4208009, 4208010, 4303041, 4304026, 4306046, 4308071, 4312018; 23) Model No. 1832210T, UPC 818392013061, Lot Numbers: 4110046, 4307048, 4308091; 24) Model No. 1832310T, UPC 10818392013075, Lot Numbers: 4110047; 25) Model No. 1852010T, UPC 818392013702, Lot Numbers: 4104083; 26) Model No. 1852110T, UPC 818392013696, Lot Numbers: 4005030, 4007049, 4103080, 4104084, 4105111, 4302024, 4308067, 4310031, 4312019, 4312102, 4912026, 19072314; b) SOL-CARE: 1) Model No. 102115SN, UPC 818392019858, Lot Numbers: 4104022; 2) Model No. 102215SN, UPC 818392019865, Lot Numbers: 4004004, 4303018, 4304057; 3) Model No. 12510SN, UPC 818392018851, Lot Numbers: 4108037, 7106031, 7109036; 4) Model No. 12558SN, UPC 818392018950, Lot Numbers: 4004005, 4104008, 4104011, 4104012, 4106034, 7107051, 7112016; 5) Model No. 12705SN, UPC 818392018967, Lot Numbers: 4004006, 7109007; 6) Model No. 13005SN, UPC 818392018974, Lot Numbers: 4004002; 7) Model No. 32110SN, UPC 818392019001, Lot Numbers: 4004031, 5101401; 8) Model No. 32115SN, UPC 818392019018, Lot Numbers: 4109051, 19072315; 9) Model No. 32210SN, UPC 818392019025, Lot Numbers: 4007046, 4301035, 4312117; 10) Model No. 32215SN, UPC 818392019032, Lot Numbers: 4301036; 11) Model No. 32310SN, UPC 818392019049, Lot Numbers: 3102005, 4004031, 4104013, 4107091, 4108035, 5104011, 5104012; 12) Model No. 32510SN, UPC 818392019063, Lot Numbers: 4007047, 4007051, 4104009, 4105096, 4105100, 4108031, 4108032, 4108036, 7111006; 13) Model No. 32558SN, UPC 818392019070, Lot Numbers: 4007048, 4007052, 4104010, 4104018; 14) Model No. 52115SN, UPC 818392018912, Lot Numbers: 4110017, 4309051; 15) Model No. 52215SN, UPC 818392018936, Lot Numbers: 4004003, 4107173; c) HENRY SCHEIN: 1) Model No. 900-7842, UPC 10304040017200, Lot Numbers: 1012089, 1012091, 1102061, 1103043, 1103044, 1103045, 1103046, 2111063, 2111064, 2203033, 2209013, 2211025, 2211026, 2307003, 2307094, 2309046, 4005032, 4005054, 4007040, 4007041; 2) Model No. 900-7843, UPC 10304040017217, Lot Numbers: 1012090, 1102062, 1103053, 2211027, 2303042, 2307005, 4003020, 4004038, 4007042, 4109001, 4109002, 4910032, 4911007; 3) Model No. 900-7844, UPC 10304040017224, Lot Numbers: 1012090, 1102062, 1103053, 2211027, 2303042, 2307005, 4003020, 4004038, 4007042, 4109001, 4109002, 4910032, 4911007
• Recalling Firm/ Manufacturer: Sol-Millennium Medical Inc.; 311 S Wacker Dr; Chicago IL 60606-6604
• For Additional Information Contact: Peter Ren; 312-545-8025
• Manufacturer Reason for Recall: Products in distribution were found by FDA to be to be substantially different from the current cleared 510(k)s with a major change or modification to the device s intended use.
• FDA Determined Cause: Other
• Action: Sol M issued a Voluntary Recall Action Letter to Distributors to its consignees on 05/09/2024 via email. The notice explained the reason for the recall and requested the following: "ACTIONS REQUIRED: 1. Examine your inventory and quarantine the affected product codes and lots subject to this recall action. 2. Distributors, please identify your customers, and notify them at once of this recall action to the distributor level. Such notification may be enhanced by including the enclosed letter (Appendix B) for your customers and Healthcare Providers (HCP s) in the field. 3. Return the enclosed Appendix B with the information via email to recalls@sol-m.com. The quarantine should be carried out to the wholesale and distributor level. Products in the field beyond the control of the distributor or wholesaler should be recalled from the field and returned to the distributor. Distributors should quarantine the products in inventory and quarantine the products received from customers until the 510(k) submissions are pending or cleared. The returned product should be quarantined in a secure location to avoid distribution based on your quality management procedures. We will provide communication with any updates as we work with the FDA."
• Distribution: US Nationwide, Czech Republic, Belgium, Portugal, Canada, Saudi Arabia, Netherland, France, Switzerland, Latvia, UK, Spain, Germany, Philippines, Australia, Malaysia, Jamaica, Slovenia, Brazil, Taiwan, Denmark, Sweden, Singapore, Romania, Poland, Barbados, Mexico, Guatemala, Chile, Ireland, Italy, Panama
• Total Product Life Cycle: 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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.