Device recall: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
Class II FDA enforcement event 89240. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Stems may have an undersized spigot bore diameter therefore separating the proximal body from the stem may not be possible without surgical delay and/or bone damage
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
DePuy Orthopaedics, Inc. started this device recall on 7 Dec 2021. The firm address in the FDA record is in Warsaw, IN. FDA put the recall in Class II. FDA event 89240 has 8 product records. The first FDA enforcement report date is 19 Jan 2022. The record gives the status Terminated, with the termination date 17 May 2024.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, Denmark, Estonia, Finland, France, Germany, Greece, Ireland, Israel, Italy, Netherlands, New Zealand,…
Recalling firm
DePuy Orthopaedics, Inc., Warsaw, IN.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
8 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0483-2022 | GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 | 28 units | Class II | Terminated | 19 Jan 2022 |
| Z-0484-2022 | GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 | 432 units | Class II | Terminated | 19 Jan 2022 |
| Z-0485-2022 | GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 | 3 units | Class II | Terminated | 19 Jan 2022 |
| Z-0486-2022 | GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 | 781 units | Class II | Terminated | 19 Jan 2022 |
| Z-0487-2022 | GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 | 3 units | Class II | Terminated | 19 Jan 2022 |
| Z-0488-2022 | GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 | 870 units | Class II | Terminated | 19 Jan 2022 |
| Z-0489-2022 | GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 | 451 units | Class II | Terminated | 19 Jan 2022 |
| Z-0490-2022 | GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 | 140 units | Class II | Terminated | 19 Jan 2022 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2021
- 900
- Share of these events in Class II
- 89%
- Product records in this event
- 8Median of the firm: 1
- Events of the firm on the register
- 59
Other events of the firm
Official channels
- FDA enforcement report Z-0483-2022The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 89240. https://recallregister.com/fda/ii/89240/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, Denmark, Estonia, Finland, France, Germany, Greece, Ireland, Israel, Italy, Netherlands, New Zealand,…
- What quantity of product is in FDA event 89240?
- The event has 8 product records. The first record gives this quantity:
28 units
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2021 have the same class?
- 89% of the 900 device events that started in 2021 are in Class II.