Bard Access Systems, Inc.: Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight

Is my product affected?

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605200; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605240; Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605300; Power-Trialysis Short-Te

• UPC 801741086953
• UPC 801741086960
• UPC 801741086977
• UPC 801741086984
• UPC 801741075087
• UPC 801741075094
• UPC 801741075100
• UPC 801741075117
• UPC 801741066054
• UPC 00801741066061
• UPC 801741066078
• UPC 801741066085
• UPC 801741100154
• UPC 801741107146
• UPC 00801741107153
• UPC 801741107412
• UPC 801741107160
• UPC 801741107177
• UPC 801741107184
• UPC 801741107191
• UPC 801741107207
• UPC 801741107214
• UPC 801741107221

Check against the official notice below — it lists the full affected range.

Hazard

this is a downstream recall of class I recall RES 98777

Details from the source

Reason for recall: this is a downstream recall of class I recall RES 98777 Distribution: US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS, NJ, AL, CA, CO, MA, NV, ID, MO, LA, WA, KY, IA, NH, NY, KS, HI, NE, MN, MT, WY, AR, RI, WV, UT, PR, DE, CT, ME, DC, ND, NM, SD Quantity: 149521 Lot/code info: REF/UDI-DI/Lot(Expiration): 5605150/801741086953/ REKQ2236(08/31/2026), REKR0948(08/31/2026), REKR3422(09/30/2026), REKR3433(09/30/2026), REKS1563(10/31/2026), REKS3564(09/30/2026), REKS3559(10/31/2026), REKT0573(11/30/2026), REKT1722(09/30/2026), REKT3057(10/31/2026), REKU1678(12/31/2026), REKV0926(01/31/2027), REKW0664(02/28/2027), REKX0410(03/31/2027), REKX1755(03/31/2027), REKY2464(03/31/2027), REKZ2323(05/31/2027), RELN2937(06/30/2027); 5605200/801741086960/ REKQ3355(8/31/2026, REKQ3362(8/31/2026), REKR0756(9/30/2026), REKR2159(9/30/2026), REKR2214(9/30/2026), REKS1550(10/31/2026), REKS1559(10/31/2026), REKS2495(10/31/2026), REKT0576(10/31/2026), REKT0579(11/30/2026), REKT2201(11/30/2026), REKT3018(11/30/2026), REKU2636(12/31/2026), REKU3679(12/31/2026), REKV2415(12/31/2026), REKW2742(2/28/2027), REKX0576(3/31/2027), REKX2423(3/31/2027), REKZ0519(5/31/2027), RELN1850(6/30/2027); 5605240/801741086977/ REKQ3367(8/31/2026), REKR0762(8/31/2026), REKS3554(8/31/2026), REKT2178(11/30/2026), REKU3687(12/31/2026), REKW0663(2/28/2027), REKW2120(2/28/2027), REKX0561(12/31/2026), REKY1369(3/31/2027), REKZ0376(5/31/2027), RELN1835(6/30/2027); 5605300/801741086984/ REKR3428(9/30/2026), REKS2486(10/31/2026), REKT3038(11/30/2026), REKV1678(10/31/2026), REKW2736(1/31/2027), REKX3721(3/31/2027), REKY2472(4/30/2027); 5615120/801741075087/ REKR0770(9/30/2026), REKR2157(9/30/2026), REKT2999(11/30/2026), REKX1764(1/31/2027), REKZ0393(2/28/2027); 5615150/801741075094/ REKQ3350(8/31/2026), REKR

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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