Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 23, 2013
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. The system is indicated for die delivery of allograft, autograft, or synthetic bone graft materials to an orthopedic surgical site. In addition, it is designed to facilitate pre-mixing of bone graft materials with the aspirate(s), I.V. fluids, blood, plasma, platelet rich plasma, bone marrow or othe
Potential for leur connector to leak or have cracks.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Harvest Technologies Corporation recalled Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft … - a moderate-severity action.
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft … was recalled by Harvest Technologies Corporation in October 23, 2013. Reason: Potential for leur connector to leak or have cracks.. Check the official notice for the remedy. Verify recall #Z-0022-2014 with the FDA Devices before acting.
The recall
Harvest Technologies Corporation issued this moderate-severity FDA Devices recall-Potential for leur connector to leak or have cracks..
- Moderate
- severity level
- Class II
- classification
- October 23, 2013
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0022-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0022-2014) was formally reported on October 23, 2013, with the manufacturer initiating the action on September 11, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Harvest Technologies Corporation is listed as the recalling firm, operating out of Plymouth, MA. Federal records list the affected scope as 730 cases (3 kits per case).
The documented reason for this recall is: Potential for leur connector to leak or have cracks. Distribution data in the federal record shows the product reached: Worldwide Distribution - USA Nationwide: TX, NJ, MI, AZ, GA, LA, ME, MD, AR, MO, VA, MN, GA, MA, NY, PA, CO, CA and in the countries of Australia, Brazil, China, Singapore, Vietnam, Dominican Republic.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
730 cases (3 kits per case)
Related Recalls
6
3 from same agency
Product description
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. The system is indicated for die delivery of allograft, autograft, or synthetic bone graft materials to an orthopedic surgical site. In addition, it is designed to facilitate pre-mixing of bone graft materials with the aspirate(s), I.V. fluids, blood, plasma, platelet rich plasma, bone marrow or other specific blood component(s) as deemed necessary by the clinical use requirements.
Reason for recall
Potential for leur connector to leak or have cracks.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0022-2014 |
| Date reported | October 23, 2013 |
| Date initiated | September 11, 2013 |
| Recalling firm | Harvest Technologies Corporation |
| Firm location | Plymouth, MA |
| Affected scope | 730 cases (3 kits per case) |
| Distribution | Worldwide Distribution - USA Nationwide: TX, NJ, MI, AZ, GA, LA, ME, MD, AR, MO, VA, MN, GA, MA, NY, PA, CO, CA and in the countries of Australia, Brazil, China, Singapore, Vietnam, Dominican Republic. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0022-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Harvest Graft Delivery System; Model Number: GDP-10 Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. The system is indicated for die delivery of allograft, autograft, or synthetic bone graft materials to an orthopedic surgical site. In addition, it is designed to facilitate pre-mixing of bone graft materials with the aspirate(s), I.V. fluids, blood, plasma, platelet rich plasma, bone marrow or other specific blood component(s) as deemed necessary by the clinical use requirements.. Recalled by Harvest Technologies Corporation. Units affected: 730 cases (3 kits per case).
Why was this product recalled? ▼
Potential for leur connector to leak or have cracks.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 23, 2013. Severity: Moderate. Recall number: Z-0022-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution - USA Nationwide: TX, NJ, MI, AZ, GA, LA, ME, MD, AR, MO, VA, MN, GA, MA, NY, PA, CO, CA and in the countries of Australia, Brazil, China, Singapore, Vietnam, Dominican Republic..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0022-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported October 23, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.