Open menu Close menu This site is intended for US Healthcare Professionals Only. This site is intended for US Healthcare Professionals Only. This site is intended for US Healthcare Professionals Only. Talk to a Live Agent Submit Question Find My MSL IUD Replacement Request Product Replacement Request Call Medical Information 1-888-842-2937 Report Adverse Event Products page Chat with a Specialist IUD REPLACEMENT BLOCK To submit an IUD Replacement Request to Bayer Medical Information, please complete the required fields below.Please submit one product replacement request per form.*Indicates required fields Physician Contact Information Healthcare provider who inserted the IUD* Healthcare Facility where Incident Occurred* Reporter name (if different) Reporter phone number (if different) Address* City* State* - Select -AlabamaAlaskaArizonaArkansasCaliforniaColoradoConnecticutDelawareDistrict of ColumbiaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaOhioOklahomaOregonPennsylvaniaRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUtahVermontVirginiaWashingtonWest VirginiaWisconsinWyomingAmerican SamoaNorthern Mariana IslandsPuerto RicoU.S. Virgin IslandsU.S. Minor Outlying Islands Zip Code* Phone* E-mail* Product Information Product Name for Replacement* - Select -Mirena® (levonorgestrel-releasing intrauterine system)Kyleena® (levonorgestrel-releasing intrauterine system)Skyla® (levonorgestrel-releasing intrauterine system) Formulation Select OneIUD Strength Lot Number* Unit Available for Return?* Yes No Information message Please keep unit for 3 weeks. You will be notified if a return is necessary. Please select why sample is unavailable - None -I only have a Picture AvailableEmpty Container/BoxSample DiscardedSample May Have ExpelledSample MisplacedUnit Still Inserted Do you need to report any Adverse Event(s) related to this Replacement Request?* Yes No Information message Please report your adverse event via the link below. You must save the "Ref#" that will appear after submitting the adverse event. When you return to this form, you must enter it into the “Adverse Event Reference Number” field to submit your request. Click here to report an adverse event and obtain your reference number Adverse Event Reference Number* Attempted Insertion Date: Description of Incident* By clicking the submit button I confirm that this is an unsolicited request. Leave this field blank