Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported March 5, 2014
Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.
Inner spherical radius of the shell is undersized.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Smith & Nephew Inc recalled Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Neph… - a moderate-severity action.
Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Neph… was recalled by Smith & Nephew Inc in March 5, 2014. Reason: Inner spherical radius of the shell is undersized.. Check the official notice for the remedy. Verify recall #Z-1066-2014 with the FDA Devices before acting.
The recall
Smith & Nephew Inc issued this moderate-severity FDA Devices recall-Inner spherical radius of the shell is undersized..
- Moderate
- severity level
- 10 units
- affected scope
- Class II
- classification
- March 5, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1066-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1066-2014) was formally reported on March 5, 2014, with the manufacturer initiating the action on January 23, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Smith & Nephew Inc is listed as the recalling firm, operating out of Memphis, TN. Federal records list the affected scope as 10 units.
The documented reason for this recall is: Inner spherical radius of the shell is undersized. Distribution data in the federal record shows the product reached: Worldwide Distribution: US Distribution to NJ and FL; and the countries of: Colombia and Costa Rica.. 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
10 units
Related Recalls
6
3 from same agency
Product description
Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.
Reason for recall
Inner spherical radius of the shell is undersized.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1066-2014 |
| Date reported | March 5, 2014 |
| Date initiated | January 23, 2014 |
| Recalling firm | Smith & Nephew Inc |
| Firm location | Memphis, TN |
| Affected scope | 10 units |
| Distribution | Worldwide Distribution: US Distribution to NJ and FL; and the countries of: Colombia and Costa Rica. |
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-1066-2014) 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? ▼
Reflection Interfit Shell, 52 MM OD, 3 HOLE, REF 71336052, QTY 1, STERILE R, Smith & Nephew, Inc. Indications for use include cemented or uncemented total hip arthroplasty for rheumatoid arthritis; osteoarthritis; post traumatic arthritis, avascular necrosis; femoral and neck fractures; osteomyelitis; fracture, dislocation of the hip; and unsuccessful cup arthroplasty, endoprosthesis, femoral osteotomy, or girdlestone resection.. Recalled by Smith & Nephew Inc. Units affected: 10 units.
Why was this product recalled? ▼
Inner spherical radius of the shell is undersized.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 5, 2014. Severity: Moderate. Recall number: Z-1066-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution: US Distribution to NJ and FL; and the countries of: Colombia and Costa Rica..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1066-2014) 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 March 5, 2014. 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.