ClearanceBrief
Recall Z-0946-2025 ยท HDQ Dilator, Cervical, Fixed Size

Sklar Instruments

ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE HEGAR DILATOR 11&12MM STRLCS25Model Number 96-0960; 2) ECONO STERILE HEGAR DILATOR 9&10MM STRL CS25Model Number 96-0961; 3) ECONO STERILE HEGAR DILATOR 7&8MM STRL CS25Model Number 96-0962; 4) ECONO STERILE HEGAR DILATOR 5&6MM STERL CS25Model Number 96-0963; 5) ECONO STERILE HEGAR DILATOR 3&4MM STERL CS25Model Number 96-0964;

DateJan 16, 2025 (initiated Dec 3, 2024)
StatusOpen, Classified
ReasonReports of various packaging issues that may result in a breach of the sterile barrier.
Root causeUnder Investigation by firm
ActionOn December 3, 2024 URGENT MEDICAL DEVICE RECALL letters were sent to customers. Action required: 1. Check your inventory for any affected product lots (see Attachment A). If you have affected product in inventory, discontinue use immediately. 2. Notify Additional Users. If you have further distributed any of the items referenced in this notification, you must notify those downstream customers of this recall. Forward a copy of this letter, along with copies of Attachment A and the Recall Acknowledgement form, for such customers to complete and return to Sklar. 3. Notify Sklar. Please complete
Quantity75 units
DistributionDomestic: Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K772229MINICLAMPS, STABILIZ., FALLOPIAN TUBE
J. Sklar Mfg. Co., Inc., Jan 3, 1978