Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 3, 2018
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Biomet Uk Ltd. recalled HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate I… - a moderate-severity action.
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate I… was recalled by Biomet Uk Ltd. in October 3, 2018. Reason: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw …. Check the official notice for the remedy. Verify recall #Z-3263-2018 with the FDA Devices before acting.
The recall
Biomet Uk Ltd. issued this moderate-severity FDA Devices recall-HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw ….
- Moderate
- severity level
- 44 units
- affected scope
- Class II
- classification
- October 3, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-3263-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-3263-2018) was formally reported on October 3, 2018, with the manufacturer initiating the action on August 9, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Biomet Uk Ltd. is listed as the recalling firm, operating out of Bridgend. Federal records list the affected scope as 44 units.
The documented reason for this recall is: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel Distribution data in the federal record shows the product reached: US Nationwide in the states of AZ, MO, NJ and NM. 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 - 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 - 40,422 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
44 units
Related Recalls
6
0 from same agency
Product description
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures
Reason for recall
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-3263-2018 |
| Date reported | October 3, 2018 |
| Date initiated | August 9, 2018 |
| Recalling firm | Biomet Uk Ltd. |
| Firm location | Bridgend |
| Affected scope | 44 units |
| Distribution | US Nationwide in the states of AZ, MO, NJ and NM |
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-3263-2018) 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? ▼
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number: 2110-135-004 Product Usage: The HipLOC Compression Hip Screw may be used primarily for fixation of bone fractures. Specific indications include open reduction and internal fixation of a wide variety of fractures of the proximal femur: intracapsular fractures, intertrochanteric fractures and subtrochanteric fractures. Recalled by Biomet Uk Ltd.. Units affected: 44 units.
Why was this product recalled? ▼
HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate barrel, can result in the lag screw not fitting through the barrel
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 3, 2018. Severity: Moderate. Recall number: Z-3263-2018.
Where was the recalled product distributed? ▼
Distribution: US Nationwide in the states of AZ, MO, NJ and NM.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-3263-2018) 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 3, 2018. 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.