Reported Aug 16, 2023 · Ongoing
Medtronic InterStim Ground Pad REF 041826
Medtronic Neuromodulation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Neuromodulation · 7000 Central Ave Ne · Minneapolis, MN · 55432-3568
Is this the product you have?
- Medtronic InterStim Ground Pad REF 041826
- Lot codes and dates
- Product Number041826
- UDI20763000343273
- Lot Number60347246
- Amount recalled
- 360 packs (36 kits of 10 packs each)
Why it was recalled
Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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