Medical Device Recall: Z-0020-06

FDA Recalls dataset · Firm: Pioneer Surgical Technology · Status: Terminated

Recall Action Class: N/A Date Initiated: 2005-07-29 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0020-06.

Recall Res Number
Z-0020-06
Recalling Firm / Manufacturer
FEI Number
1000115331
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2005-07-29
Date Posted
2005-10-07
Date Terminated
2005-10-25
Product Code
NKB
Event Number
32949
Product Quantity
110
Product Description Pioneer Surgical brand Quantum Spinal Rod System Polyaxial Screw, length 45 mm; Catalog number 10-575-PA-45.

Reason for Recall Screw may be incorrectly etched as to length.

Action Details Consignees were notified by letter dated 7/29/05 to inspect stocks in storage and at point of use locations hand for correct length and that a firm representative would visit them to pick up any mis-etched product.

Distribution Pattern Nationwide.

Code Information / Serial Numbers Lot 306507.

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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