Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/8’’
Medical device recall Z-3074-2024. Published in FDA’s Enforcement Report on Sep 18, 2024.
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 Sep 18, 2024. Copied from openFDA on Oct 20, 2026.
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?
Products in distribution were found by FDA to be to be substantially different from the current cleared 510(k)s with a major change or modification to the device s intended use.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/8’’, Model No. 181025, UPC 818392014884; 2) SOL-M 3ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1831815B, UPC 818392011593; 3) SOL-M 5ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1851815B, UPC 818392011609; 4) SOL-M 10ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1811815B, UPC 818392011616;
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/8’’, Model No. 181025, UPC 818392014884, Lot Numbers: 4302039, 4308074; 2) SOL-M 3ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model…
Every code shown here, 1,993 characters
Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M 1ml TB Syringe w/Fixed Needle 25G*5/8’’, Model No. 181025, UPC 818392014884, Lot Numbers: 4302039, 4308074; 2) SOL-M 3ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1831815B, UPC 818392011593, Lot Numbers: 4103001, 4106151, 4111045, 4304001; 3) SOL-M 5ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1851815B, UPC 818392011609, Lot Numbers: 4103001, 4106151, 4111045, 4304001; 4) SOL-M 10ml Luer Lock Syringe w/Blunt Fill Needle 18G*1 1/2’’, Model No. 1811815B, UPC 818392011616, Lot Numbers: 4103001, 4106151, 4111045, 4304001; b) SOL-CARE: 1) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 23G*1’’, Model No. 12310SN, UPC 810018098148, Lot Numbers: 4108032, 7107049; 2) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 23G*1 1/2’’, Model No. 12315SN, UPC 810018098827, Lot Numbers: 4110077; 3) SOL-CARE 1ml Luer Lock Syringe w/Safety Needle 25G*1 1/2’’, Model No. 12515SN, UPC 810018098155, Lot Numbers: 4108033, 7107048; 4) SOL-CARE 3ml Luer Lock Syringe w/Safety Needle 25G*1 1/2’’, Model No. 32515SN, UPC 810018098162, Lot Numbers: 4108034, 4109052; c) MEDLINE: 1) MEDLINE 1ml Luer Lock Syringe w/Safety Needle 23G*1, Model No. SYRS101235F, UPC 10888277222298, Lot Numbers: 1008006, 1011003, 1011012, 1103028, 1105073, 1909004, 1910005, 1910037, 1911016, 19061701; 2) MEDLINE 1ml Luer Lock Syringe w/Safety Needle 25G*1, Model No. SYRS101255F, UPC 10888277222472, Lot Numbers: 1009007, 1009014, 1011013, 1011023, 1102018, 1105074, 1910038, 1911017, 1912007; 3) MEDLINE 1ml Luer Lock Syringe w/Safety Needle 27G*1/2, Model No. SYRS101272F, UPC 10888277222489, Lot Numbers: 1001014, 1001016, 1009006, 1010004, 1012006, 19041693, 19052315, 19061702, 19071701; 4) MEDLINE 1ml Luer Lock Syringe w/Safety Needle 30G*1/2, Model No. SYRS101392F, UPC 10888277222502, Lot Numbers: 1009041, 1103029, 1109049, 1110059, 1111051; 5) MEDLINE 3ml Luer Lock Syringe w/Safety Needle 20G*1, Model No. SYRS103205, UPC…
FDA’s list runs to 9,275 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.
Barcodes and drug codes
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UPC
818392014884 -
UPC
818392011593 -
UPC
818392011609 -
UPC
818392011616 -
UPC
810018098148 -
UPC
810018098827 -
UPC
810018098155 -
UPC
810018098162 -
UPC
10888277222298 -
UPC
10888277222472 -
UPC
10888277222489 -
UPC
10888277222502 -
UPC
10888277222519 -
UPC
10888277222526 -
UPC
10888277222533 -
UPC
10888277222540 -
UPC
10888277222557 -
UPC
10888277222564 -
UPC
10888277222571 -
UPC
10888277222588 -
UPC
10888277222595 -
UPC
10888277222632 -
UPC
10888277222670 -
UPC
10888277222694 -
UPC
10888277222892 -
UPC
1092253025132 -
UPC
10192253025149 -
UPC
10192253025156 -
UPC
10192253025163 -
UPC
10192253025170 -
UPC
10192253025187 -
UPC
10192253025194 -
UPC
10192253025200 -
UPC
10192253025217 -
UPC
10192253025224 -
UPC
10192253025231 -
UPC
10192253025248 -
UPC
10192253025225 -
UPC
10304040017057 -
UPC
10304040017064 -
UPC
10304040017071 -
UPC
10304040017088 -
UPC
10304040017095 -
UPC
10304040017101 -
UPC
10304040017118 -
UPC
10304040017125 -
UPC
10304040017149 -
UPC
10304040017194
As FDA’s description and codes give them; the UPCs written as digits only.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US Nationwide, Czech Republic, Belgium, Portugal, Canada, Saudi Arabia, Netherland, France, Switzerland, Latvia, UK, Spain, Germany, Philippines, Australia, Malaysia, Jamaica, Slovenia, Brazil, Taiwan, Denmark, Sweden, Singapore, Romania, Poland, Barbados, Mexico, Guatemala, Chile, Ireland, Italy, Panama
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, 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 May 9, 2024.
- FDA classified it on Sep 6, 2024.
- FDA’s Enforcement Report published it on Sep 18, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Sol-Millennium Medical Inc., of Chicago, IL.
- 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 9,275 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.