SafeStep Huber Needle Set
Medical device recall Z-2671-2020. Published in FDA’s Enforcement Report on Jul 29, 2020.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jul 29, 2020. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Not named no state, in where it went
- 5,296,132 total how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
SafeStep Huber Needle Set; Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382)
5,296,132 total, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI…
Every code shown here, 2,000 characters
Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382). Lot Numbers: ASCYF001 ASCYF017 ASDRF018 ASDRF031 ASDRF040 ASDSF065 ASDSF070 ASDTF004 ASDTF007 ASDVF048 ASDVF054 ASDXF058 ASDXF060 ASDXF066 ASDYF071 ASDYF077 ASDYF098 ASDZF010 ASDZF017 ASDZF024 ASDZF035 ASDZF036 ASDZF046 ASDZF071 ASDZF081 ASDZF093 ASENF002 ASERF025 ASERF032 ASCYF015 ASCYF016 ASCZF027 ASDRF043 ASDRF044 ASDRF054 ASDRF055 ASDRF056 ASDVF058 ASDVF063 ASDXF020 ASDXF045 ASENF011 ASENF014 ASERF004 ASCYF089 ASCYF090 ASCYF091 ASCYF092 ASCZF009 ASCZF010 ASCZF011 ASCZF022 ASCZF023 ASCZF039 ASCZF040 ASCZF045 ASCZF054 ASDPF016 ASDQF035 ASDQF054 ASDQF055 ASDQF060 ASDQF064 ASDRF006 ASDRF014 ASDRF019 ASDRF032 ASDRF039 ASDRF069 ASDRF073 ASDRF087 ASDRF098 ASDSF003 ASDSF010 ASDSF016 ASDSF019 ASDSF022 ASDSF033 ASDSF047 ASDSF050 ASDSF057 ASDSF061 ASDSF069 ASDTF005 ASDTF008 ASDTF022 ASDVF051 ASDVF060 ASDVF071 ASDVF079 ASDVF091 ASDWF004 ASDWF013 ASDWF018 ASDWF034 ASDWF035 ASDWF036 ASDWF040 ASDWF041 ASDWF042 ASDWF046 ASDWF047 ASDWF048 ASDWF052 ASDWF053 ASDWF054 ASDWF058 ASDWF059 ASDWF060 ASDWF080 ASDWF090 ASDWF099 ASDWF121 ASDWF126 ASDXF006 ASDXF014 ASDXF053 ASDXF063 ASDXF070 ASDXF078 ASDXF092 ASDXF096 ASDXF101 ASDXF103 ASDXF106 ASDYF001 ASDYF004 ASDYF006 ASDYF009 ASDYF010 ASDYF015 ASDYF019 ASDYF023 ASDYF029 ASDYF033 ASDYF037 ASDYF044 ASDYF050 ASDYF054 ASDYF060 ASDYF061 ASDYF074 ASDYF082 ASDYF093 ASDZF004 ASDZF013 ASDZF058 ASDZF069 ASEPF012 ASEPF015 ASEPF017 ASEPF021 ASEQF001 ASEQF022 ASEQF026 ASEQF031 ASEQF066 ASEQF083 ASEQF092 ASEQF110 ASEQF132 ASERF013 ASERF022 ASDNF034 ASDNF049 ASDNF055 ASDPF015 ASDPF017 ASDPF021 ASDPF024 ASDPF025 ASDPF026 ASDQF017 ASDRF066 ASDUF120 ASDVF004 ASDVF009 ASDVF013 ASDVF016…
FDA’s list runs to 2,857 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jun 19, 2020.
- FDA classified it on Jul 18, 2020.
- FDA’s Enforcement Report published it on Jul 29, 2020.
- FDA terminated it on Jul 29, 2022.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Becton Dickinson & Company, of Franklin Lakes, NJ.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 2,857 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.