Reported Mar 25, 2020 · Ongoing
Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as…
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
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 Inc., Cardiac Rhythm and Heart Failure (CRHF) · 8200 Coral Sea St Ne · Mounds View, MN · 55112-4391
Is this the product you have?
- Medtronic CareLink 2090 Programmer. Used to interrogate and program Medtronic and Vitatron implantable devices, such as pacemaker/ICD/CRT.
- Lot codes and dates
- Product Number 2090; All Serial Numbers
- Known Model Numbersa. Model Number 2090
- GTIN (Lot Numbers)
1,048 of 1,048 codes
00721902546341 (PKK002840R)00721902246234 (PKK012608R)00721902246234 (PKK013358R)00721902569517 (PKK017436R)00613994580955 (PKK204009R)00643169537828 (PKK001072R)00613994175397 (PKK001076R)00613994175397 (PKK001135R)00613994175397 (PKK001172R)00613994175120 (PKK001321R)00613994175106 (PKK001322R)00721902246234 (PKK001324R)00721902246227 (PKK001327R)00613994175212 (PKK001328R)00613994175106 (PKK001331R)00643169537828 (PKK001332R)00721902246234 (PKK001335R)00613994175144 (PKK001348R)00721902246227 (PKK001352R)00613994175076 (PKK001358R)00613994581075 (PKK001359R)00721902246234 (PKK001361R)00643169537828 (PKK001362R)00613994175397 (PKK001364R)00613994581204 (PKK001367R)00613994175267 (PKK001373R)00613994175397 (PKK001376R)00613994175120 (PKK001382R)00613994175397 (PKK001386R)00613994175083 (PKK001387R)00643169537828 (PKK001390R)00613994175397 (PKK001395R)00613994581235 (PKK001398R)00613994175106 (PKK001400R)00721902246234 (PKK001401R)00613994175212 (PKK001403R)00613994175106 (PKK001407R)00613994136534 (PKK001409R)00613994175120 (PKK001410R)00613994581235 (PKK001411R)00613994581228 (PKK001420R)00613994136527 (PKK001421R)00613994136527 (PKK001422R)00613994175120 (PKK001425R)00613994175182 (PKK001431R)00643169440166 (PKK001433R)00613994175076 (PKK001437R)00613994175083 (PKK001444R)00613994175076 (PKK001448R)00613994581228 (PKK001454R)00613994175380 (PKK001459R)00613994175380 (PKK001460R)00613994175090 (PKK001473R)00613994175083 (PKK001474R)00613994175106 (PKK001476R)00613994136527 (PKK001480R)00613994581075 (PKK001484R)00613994175212 (PKK001485R)00613994175120 (PKK001487R)00613994175106 (PKK001488R)
- Amount recalled
- 23,180 devices
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Medtronic Conexus Telemetry has been determined to contain two primary cyber vulnerabilities: improper access control and the cleartext transmission of sensitive information.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Medtronic Inc., Cardiac Rhythm and Heart… recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.