CLASS II ONGOING Device recall · Reported 8 Feb 2023 · FDA Enforcement Report
Catalog Number / Product Description 0601600 2.7F Broviac recalled
Bard Peripheral Vascular is recalling Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter, distributed nationwide in the US. The recall was initiated on 4 Jan 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1051-2023
- FDA event ID
- 91327
- Recalling firm
- Bard Peripheral Vascular, Tempe, AZ
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 4 Jan 2023
- FDA classified
- 1 Feb 2023
- Reported
- 8 Feb 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Heart & Vascular Devices
Timeline
| 4 Jan 2023 | Recall initiated by company | |
| 1 Feb 2023 | Classified by FDA | +28 days |
| 8 Feb 2023 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable).
Product as listed by the FDA
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter Repair Kit 0601620 6.6F Broviac CV Catheter Repair Kit 0601630 9.6F Hickman CV Catheter Repair Kit 0601680 Hickman / Leonard CV Catheter Repair Kit (all except 13.5F) 0601690 Hickman / Leonard CV Catheter Repair Kit (all except 13.5F) 0601700 9F Hickman CV Catheter Repair Kit 0601710 12F Hickman CV Catheter Repair Kit 0601730 Hickman / Leonard CV Catheter Repair Kit (all except 13.5F) 0601740 12.5F Hickman CV Catheter Repair Kit 0601750 10F Leonard CV Catheter Repair Kit 0601760 7F Hickman CV Catheter Repair Kit 0601790 10F Hickman CV Catheter Repair Kit
Where it was distributed
Worldwide Distribution: U.S.(nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV; OUS (foreign) countries of: Australia, Belgium, Canada, Hong Kong and Japan. O.U.S.: Australia, Belgium, Canada, Hong Kong, and Japan.
Nationwide AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusetts
Questions about this recall
Is Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter recalled?
Yes. Bard Peripheral Vascular recalled Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter on 4 Jan 2023. The recall is Class II and its status is Ongoing. Recall number Z-1051-2023.
Why was it recalled?
Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable).
Which lots are affected?
Catalog Numbers/Lot-Serial Numbers/UDI Code: 0601610 / REFX4541 / (01)00801741036385(17)230930(10)REFX4541 0601610 / REFX5636 / (01)00801741036385(17)240930(10)REFX5636 0601610 / REFY2820 / (01)00801741036385(17)230930(10)REFY2820 0601610 / REGP0198 / (01)00801741036385(17)241231(10)REGP0198 0601610 / REGP2720 / (01)00801741036385(17)250131(10)REGP2720 0601610 / REGQ1144 / (01)00801741036385(17)250228(10)REGQ1144 0601620 / REES0680 / (01)00801741074479(17)230430(10)REES0680 0601620 / REEU0726 / (01)00801741074479(17)230630(10)REEU0726 0601620 / REEU1536 / (01)00801741074479(17)230630(10)REEU1536 0601620 / REEU3300 / (01)00801741074479(17)230630(10)REEU3300 0601620 / REEV1906 / (01)00801741074479(17)230731(10)REEV1906 0601620 / REFX4543 / (01)00801741074479(17)230930(10)REFX4543 0601630 / REEQ0746 / (01)00801741036408(17)230228(10)REEQ0746 0601630 / REGN2382 / (01)00801741036408(17)241231(10)REGN2382 0601630 / REGQ1143 / (01)00801741036408(17)250228(10)REGQ1143 0601680 / REER3749 / (01)00801741036415(17)230331(10)REER3749 0601680 / REEU1626 / (01)00801741036415(17)230630(10)REEU1626 0601690 / REES0716 / (01)00801741036422(17)230131(10)REES0716 0601690 / REFX1172 / (01)00801741036422(17)230131(10)REFX1172 0601690 / REFY0874 / (01)00801741036422(17)230131(10)REFY0874 0601700 / REES2549 / (01)00801741036439(17)230430(10)REES2549 0601700 / REGQ1154 / (01)00801741036439(17)230731(10)REGQ1154 0601710 / REFY2852 / (01)00801741036446(17)231031(10)REFY2852 0601730 / REGQ1174 / (01)00801741036453(17)240229(10)REGQ1174 0601740 / REFZ0223 / (01)00801741036460(17)230930(10)REFZ0223 0601750 / REFY0744 / (01)00801741036477(17)230731(10)REFY0744 0601760 / REEU1534 / (01)00801741036484(17)230630(10)REEU1534 0601790 / REFW1651 / (01)00801741036514(17)231031(10)REFW1651 7741700 / REET0877 / (01)00801741036798(17)240131(10)REET0877 7741800 / REER0703 / (01)00801741036804(17)240531(10)REER0703 7741800 / REFW3156 / (01)00801741036804(17)250131(10)REFW3156 0601600 / REES06790 / (01)00801741036378(17)220831(10)REES0679 0601600 / REES2528 / (01)00801741036378(17)220831(10)REES2528 0601600 / REES3456 / (01)00801741036378(17)220831(10)REES3456 0601610 / REEQ1683 / (01)00801741036385(17)220831(10)REEQ1683 0601610 / REEQ4180 / (01)00801741036385(17)220831(10)REEQ4180 0601610 / REER3748 / (01)00801741036385(17)220831(10)REER3748 0601610 / REES0715 / (01)00801741036385(17)220831(10)REES0715 0601610 / REET3287 / (01)00801741036385(17)220831(10)REET3287 0601620 / REEQ2751 / (01)00801741074479(17)220831(10)REEQ2751 0601620 / REEQ4141 / (01)00801741074479(17)220831(10)REEQ4141 0601620 / REER3694 / (01)00801741074479(17)220831(10)REER3694 0601620 / REET3269 / (01)00801741074479(17)220831(10)REET3269 0601630 / REEU0729 / (01)00801741036408(17)220831(10)REEU0729 0601630 / REEU3297 / (01)00801741036408(17)220831(10)REEU3297 0601690 / REEU0727 / (01)00801741036422(17)220831(10)REEU0727 0601700 / REER3695 / (01)00801741036439(17)220831(10)REER3695 0601710 / REER3750 / (01)00801741036446(17)220831(10)REER3750 0601710 / REEU3314 / (01)00801741036446(17)220831(10)REEU3314 0601740 / REEU3298 / (01)00801741036460(17)220831(10)REEU3298 0601750 / REEU0730 / (01)00801741036477(17)220831(10)REEU0730 0601750 / REEU1608 / (01)00801741036477(17)220831(10)REEU1608 0601760 / REER3696 / (01)00801741036484(17)220831(10)REER3696 0601760 / REES3457 / (01)00801741036484(17)220831(10)REES3457 0601760 / REET2794 / (01)00801741036484(17)220831(10)REET2794 0601760 / REEU1184 / (01)00801741036484(17)220831(10)REEU1184
Where was it sold?
Worldwide Distribution: U.S.(nationwide): AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV; OUS (foreign) countries of: Australia, Belgium, Canada, Hong Kong and Japan. O.U.S.: Australia, Belgium, Canada, Hong Kong, and Japan.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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