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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

The Anspach Effort, Inc.: Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed.; The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.

Agency Publication Date: September 16, 2016
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Affected Products

Product: G1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.

Material L-7B-G1 Batch K043113667

Lot Numbers:
K043113667
Product: G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.

Material M-3DC-2-G1 Batch J313108568 & J316017637

Lot Numbers:
J313108568
Product: G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium.

Material M-3SB-2-G1 Batch J316017640

Lot Numbers:
J316017640
Product: G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.

Material M-6DC-2-G1 Batch J313108573 and J 316017642

Lot Numbers:
J313108573

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 75121
Status: Resolved
Manufacturer: The Anspach Effort, Inc.
Manufactured In: United States
Units Affected: 4 products (177; 88; 63; 69)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.