TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DF, (BiD Curve D-F), REF A-TFSE-DF; cardi...
FDA Device Recall #Z-0111-2026 - Class I, September 10, 2025
Recall Summary
| Recall Number | Z-0111-2026 |
| Classification | Class I - Serious risk |
| Date Initiated | September 10, 2025 |
| Status | Ongoing |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Abbott |
| Location | Plymouth, MN |
| Product Type | Devices |
| Quantity | 85803 units |
Product Description
TactiFlex Sensor Enabled Ablation Catheter, 8F, 115 cm, DF, (BiD Curve D-F), REF A-TFSE-DF; cardiac catheter
Reason for Recall
Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
Distribution Pattern
Worldwide
Lot / Code Information
GTIN 05415067034571, Batch Numbers: 8707463, 8728375, 8848814, 8849428, 8856153, 8859777, 8930724, 8948407, 9085267, 9134878, 9139151, 9151701, 9154571, 9170156, 9172378, 9202684, 10005870, 10014420, 10014422, 10035838, 10060049, 10067495, 10074488, 10093061, 10095119, 10133240, 10143719, 10146336, 10150246, 10150248, 10158750, 10163256, 10168649, 10175479, 10191672, 10206135, 10219459, 10246287, 10250075, 10259721, 10266993, 10268128, 10278549, 10278947, 10278998, 10279023, 10279962, 10282364, 10284613, 10286135, 10299761, 10301720, 10301724, 10302971, 10310965, 10313193, 10321650, 10321684, 10330213, 10334312, 10337388, 10343800, 10346421, 10347095, 10350600, 10356054, 10356057, 10358260, 10358261, 10358263, 10358912, 10359408, 10359726, 10364782, 10368136, 10369950, 10373269, 10383386, 10392552, 10398359, 10399262, 10399266, 10401107, 10401352, 10405601, 10406221, 10413503, 10419427, 10420466, 10423182, 10424553, 10429934, 10433340, 10441923, 10442325, 10446371, 10466941, 10467483, 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10936492, 10936499, 10938539, 10941086, 10941569, 10952592, 10954107, 10954511, 10958355, 10959849, 10959850, 10967027, 10967028, 10967388, 10968503, 10968505, 10968738, 10969028, 10970142, 10970338, 10970349, 10970358, 10972424, 10972425, 10972426, 10972427, 10972849, 10972861, 10972865, 10974479, 10974480, 10974665, 10974681, 10976227, 10976255, 10976474, 10976778, 10976807, 10976987, 10978136, 10978678, 10978683, 10980067, 10980199, 10980898, 10983203, 10983441, 10983449, 10983892, 10985075, 10985378, 10985509, 10987475, 10988895, 10989409, 10990012, 10990076, 10990758, 10991009, 10993347, 10993686, 11037069, 11047469, 11047470, 11047471, 11065005, 11065006, 11065007, 11065008, 11065009, 11065010, 11065011, 11065012, 11071628, 10965759, 10972864, 10974062, 10976804, 10978680, 10978681, 10980198, 10980889, 10982507, 10983202, 10983426, 10986129, 10989279, 10989392, 10990760, 10990761, 10992107, 10993351, 10952598, 10965387, 10965405, 10966225, 10972964, 10974066, 10978510, 10980893, 10980895, 10985076, 10970654, 10970670, 10985073, 10987683.
Other Recalls from Abbott
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0109-2026 | Class I | TactiFlex Sensor Enabled Ablation Catheter, 8F,... | Sep 10, 2025 |
| Z-0112-2026 | Class I | TactiFlex Sensor Enabled Ablation Catheter, 8F,... | Sep 10, 2025 |
| Z-0110-2026 | Class I | TactiFlex Sensor Enabled Ablation Catheter, 8F,... | Sep 10, 2025 |
| Z-0113-2026 | Class I | TactiFlex Sensor Enabled Ablation Catheter, 8F,... | Sep 10, 2025 |
| Z-1643-2025 | Class II | Amplatzer TorqVue LP Delivery System (TVLP), Mo... | Mar 17, 2025 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic, removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency, Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.