Severity
Moderate
ModerateClass IIOngoing
FDA Devices recall · Reported March 6, 2024
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Waldemar Link GmbH & Co. Kg (Mfg Site) recalled LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for … - a moderate-severity action.
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for … was recalled by Waldemar Link GmbH & Co. Kg (Mfg Site) in March 6, 2024. Reason: Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference …. Check the official notice for the remedy. Verify recall #Z-1219-2024 with the FDA Devices before acting.
The recall
Waldemar Link GmbH & Co. Kg (Mfg Site) issued this moderate-severity FDA Devices recall-Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference ….
- Moderate
- severity level
- Class II
- classification
- March 6, 2024
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1219-2024 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1219-2024) was formally reported on March 6, 2024, with the manufacturer initiating the action on January 22, 2024. It is classified under Moderate severity (Class II), with a current status of Ongoing. Waldemar Link GmbH & Co. Kg (Mfg Site) is listed as the recalling firm, operating out of Norderstedt. The number of affected units is not disclosed in the agency filing, which is common for drug and food recalls where lot-level tracking supersedes unit counts.
The documented reason for this recall is: Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery Distribution data in the federal record shows the product reached: Worldwide - US Nationwide distribution in the states of IL, IN, FL, WA and the countries of Germany, Switzerland.. 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
Unknown
Related Recalls
6
3 from same agency
Product description
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12
Reason for recall
Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-1219-2024 |
| Date reported | March 6, 2024 |
| Date initiated | January 22, 2024 |
| Recalling firm | Waldemar Link GmbH & Co. Kg (Mfg Site) |
| Firm location | Norderstedt |
| Affected scope | Not disclosed |
| Distribution | Worldwide - US Nationwide distribution in the states of IL, IN, FL, WA and the countries of Germany, Switzerland. |
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-1219-2024) 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? ▼
LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12. Recalled by Waldemar Link GmbH & Co. Kg (Mfg Site).
Why was this product recalled? ▼
Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 6, 2024. Severity: Moderate. Recall number: Z-1219-2024.
Where was the recalled product distributed? ▼
Distribution: Worldwide - US Nationwide distribution in the states of IL, IN, FL, WA and the countries of Germany, Switzerland..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1219-2024) 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 6, 2024. 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.