Spinal Concepts, Inc 1757-1: Compressor/Distractor Instrument (aka Plate Distractor Forceps), and product literature. Devices are manufactured by Spinal Concepts, Inc., An Abbott Laboratories Company Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
1757-1: Compressor/Distractor Instrument (aka Plate Distractor Forceps), and product literature. Devices are manufactured by Spinal Concepts, Inc., An Abbott Laboratories Company
Brand
Spinal Concepts, Inc
Lot Codes / Batch Numbers
All lots
Products Sold
All lots
Spinal Concepts, Inc is recalling 1757-1: Compressor/Distractor Instrument (aka Plate Distractor Forceps), and product literature. De due to Design has insufficient articulating distance between the two component plates to prevent disassociation in vivo.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Design has insufficient articulating distance between the two component plates to prevent disassociation in vivo.
Recommended Action
Per FDA guidance
The firm initiated the recall via telephone on 03/01/2004 to all distributors followed up by recall letter on 03/05/2004.
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