Bard Peripheral Vascular Inc TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 15G x 79mm
Brand
Bard Peripheral Vascular Inc
Lot Codes / Batch Numbers
Catalog Number/UDI: TIN3018/(01)10885403043819(17)241031(10)0001330956, TIN3015/(01)10885403043796(17)241031(10)0001331229, Serial Numbers: 0001330956, 0001331229
Products Sold
Catalog Number/UDI: TIN3018/(01)10885403043819(17)241031(10)0001330956; TIN3015/(01)10885403043796(17)241031(10)0001331229; Serial Numbers: 0001330956; 0001331229;
Bard Peripheral Vascular Inc is recalling TIN3018 Illinois Bone Marrow Aspiration/Intraosseous Infusion Needle 18G x 79mm TIN3015 Illinois Bon due to Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to complaints received regarding incomplete/open packaging seals potentially causing product to non-sterile.
Recommended Action
Per FDA guidance
On 07/15/2021, the firm sent an "URGENT MEDICAL DEVICE CORRECTION" Notification via FedEx to customers/distributors informing them that the firm has confirmed a complaint regarding an open packaging seal, breaking the sterile barrier. Customers are instructed to: 1. Please check all inventory locations within their institution for the product listed in Table A and immediately destroy all affected product remaining in their possession. The product should have the sterile barrier broken and destroyed per their local facilitys destruction process. 2. Share this notice with any users of the product within their facilities to ensure they are also aware of this Urgent Medical Device Correction. 3. If they purchased this product from a distributor, contact their distributor for further instructions. 4. Complete and return the attached Customer Response Form to the BD contact noted on the form confirming acknowledgement of the notification, whether or not they have any affected product, so that the Recalling Firm may acknowledge their receipt of this notification and process your replacement. 5. Please contact their Recalling Firm's representative to assist in this process or they may also contact the number below for further assistance. The Recalling Firm will: 1. Issue replacements for all customers affected by the recall following receipt of the completed Customer Response Form. 2. taken action to prevent recurrence of this product issue. For questions or assistance contact (Recall Questions/Product Complaints/Technical Questions): North American Regional Complaint Center 1-844-8BD- LIFE (1-844-823-5433), Say Recall when prompted M-F 8am - 5pm CT
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026