Reported Oct 13, 2021 · Ongoing

REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI:…

Bard Peripheral Vascular Inc.

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: Bard Peripheral Vascular Inc · 1625 W 3rd St Bldg 1 · Tempe, AZ · 85281-2438

Is this the product you have?

  • REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO
  • UDI10885403043796
Lot codes and dates
  • Lot/Serial Number - Exp
  • Date

    241 of 241 codes

    • 963162 6/30/2021
    • 967672 6/30/2021
    • 978229 7/31/2021
    • 986594 7/31/2021
    • 988075 7/31/2021
    • 991067 8/31/2021
    • 994373 8/31/2021
    • 996570 8/31/2021
    • 998004 8/31/2021
    • 998332 8/31/2021
    • 1000061 8/31/2021
    • 1004858 9/30/2021
    • 1005204 9/30/2021
    • 1007650 9/30/2021
    • 1010791 9/30/2021
    • 1013939 9/30/2021
    • 1017379 10/31/2021
    • 1035580 11/30/2021
    • 1035581 11/30/2021
    • 1038740 11/30/2021
    • 1044131 12/31/2021
    • 1049259 12/31/2021
    • 1050881 12/31/2021
    • 1052628 12/31/2021
    • 1057742 1/31/2022
    • 1059045 1/31/2022
    • 1061515 1/31/2022
    • 1065338 1/31/2022
    • 1066413 1/31/2022
    • 1066484 1/31/2022
    • 1068754 2/28/2022
    • 1069385 2/28/2022
    • 1072036 2/28/2022
    • 1072932 2/28/2022
    • 1076214 2/28/2022
    • 1078134 2/28/2022
    • 1078406 2/28/2022
    • 1080547 2/28/2022
    • 1082456 2/28/2022
    • 1085984 3/31/2022
    • 1086606 3/31/2022
    • 1087768 3/31/2022
    • 1088480 3/31/2022
    • 1089329 3/31/2022
    • 1089500 3/31/2022
    • 1090412 3/31/2022
    • 1092057 3/31/2022
    • 1094384 3/31/2022
    • 1095382 4/30/2022
    • 1097231 4/30/2022
    • 1097282 4/30/2022
    • 1098267 4/30/2022
    • 1099427 4/30/2022
    • 1102009 4/30/2022
    • 1109455 5/31/2022
    • 1110142 5/31/2022
    • 1112821 5/31/2022
    • 1113754 5/31/2022
    • 1116187 5/31/2022
    • 1121054 5/31/2022

Where it was sold

Why it was recalled

Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.

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.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:50 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.