SEASPINE ORTHOPEDICS CORPORATION Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: No
Brand
SEASPINE ORTHOPEDICS CORPORATION
Lot Codes / Batch Numbers
Lot Code: UDI 10889981216368 Lot Numbers TT0190H, TT0191H
Products Sold
Lot Code: UDI 10889981216368 Lot Numbers TT0190H, TT0191H
SEASPINE ORTHOPEDICS CORPORATION is recalling Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-00301 due to Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Insufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
Recommended Action
Per FDA guidance
On June 4, 2024, SeaSpine Orthopedics issued a "Urgent Medical Device Recall" Notification via E-Mail to affected consignees. SeaSpine Orthopedics ask consignees to take the following actions: We request that you return the affected part to SeaSpine s Carlsbad facility for evaluation and potential rework. To support your upcoming cases, a replacement Vu aPod Prime NM Angled Awl will be sent (PN: 33-40-1028). Additionally, please continue to utilize the loaner pool. Please use the attached label to return the inventory in your possession at your earliest convenience. Once the inventory has been returned, please acknowledge via DocuSign.
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 noticeDistribution
As reported by FDA
AZ, CA, CO, FL, GA, IL, IN, MI, MN, MO, MT, NV, PA, SD, TN, TX, VA, WA
Page updated: Jan 10, 2026