SAFE-T-FILL Micro Capillary Blood Collection, 125 L… recallZ-0372-2026 · ASP Global, LLC. dba Anatomy Supply Partners, LLC. · initiated May 5, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from ASP Global, LLC. dba Anatomy Supply Partners, LLC. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
All RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when used with Magellan Diagnostics LeadCare Testing Systems. False positive lead results may cause delayed results and additional unnecessary testing.
FDA root cause category: Component design/selection
What the company is doing
Starting on 5//5/2025 customers were informed that there had been reports of falsely elevated blood lead levels associated with the use of affected micro capillary tubes for lead testing when used with Magellan LeadCare Testing Systems. On 9/8/2025, recall notices were emailed to customers who were asked to do the following: Discontinue use of the recalled products immediately. b) Quarantine any remaining inventory to prevent further use. c) Dispose remaining inventory in accordance with local regulations or notify firm at [email protected] for return authorization and disposal assistance. d) Complete and return the enclosed Recall Response Form to confirm receipt and actions to [email protected] Distributors are asked to notify their customers of the recall or to forward their customer information to the recalling firm so they might notify these customers.
Recall details
- Recall number
- Z-0372-2026
- Status
- Open, Classified
- Initiated by the company
- May 5, 2025
- Posted by the FDA
- Oct 27, 2025
- Recalling firm
- ASP Global, LLC. dba Anatomy Supply Partners, LLC.
- Quantity
- 4,272,858
- Product code
- JKA
- FDA submissions
- K981973
- Distribution
- Worldwide - US Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI and the country of CA.
Product description
SAFE-T-FILL Micro Capillary Blood Collection, 125 L Prepared with Dipotassium EDTA Purple, Model: 07 6011; SAFE-T-FILL Micro Capillary Blood Collection, 125 L Prepared with Dipotassium EDTA Self-sealing Cap, Purple, Model: 07 6013; SAFE-T-FILL Micro Capillary Blood Collection, 200 L Prepared with Dipotassium EDTA Purple, Model: 07 7051; SAFE-T-FILL Micro Capillary Blood Collection, 150 L Prepared with Dipotassium EDTA Purple, Model: 07 7052; SAFE-T-FILL Micro Capillary Blood Collection, 300 L Prepared with Dipotassium EDTA Purple, Model: 07 7053; SAFE-T-FILL Micro Capillary Blood Collection, 200 L Prepared with Dipotassium EDTA Purple, Model: 07 7056; SAFE-T-FILL Micro Capillary Blood Collection, 200 L Prepared with Dipotassium EDTA Flat Bottom Microtube, Purple, Model: 07 7058 SAFE-T-FILL End-to-End Capillary Tubes, 30 L; Plastic, Prepared with EDTA Dipotassium Model: 06 0910
Code information (models, lots, serial numbers)
Show the full code information (1k characters)
Model/UDI-DI/Lots: 07 6011/10643351000014/23H4110, 23I4017, 23I4051, 23J4031, 23K4058, 23K4059, 23L4082, 24A4103, 24B4186, 24B4187, 24D4015, 24E4138, 24E4139, 24H4121, 24I4317, 24I4328, 24J4041, 24J4137, 24J4138, 24J4233, 24J4316, 24J4348; 07 6013/10643351000021/23H4111, 23I4018, 24B4188, 24H4125, 25B4099; 07 7051/10643351000038/23H4157, 23I4020, 23I4374, 23J4033, 23K4060, 23L4083, 24A4104, 24B4190, 24D4016, 24E4140, 24F4053, 24I4321, 24J4043, 24J4139, 24J4237, 24L4001, 25B4107; 07 7052/10643351000045/23H4113, 23I4021, 23J4034, 24A4105, 24D4017, 24F4052, 24H4126, 24I4323, 24J4042, 24J4140, 24J4338, 24J4355, 25B4108; 07 7053/10643351000052/23I4022, 23J4035, 23L4084, 24D4018, 24E4132, 24F4192, 25B4106; 07 7056/10643351000069/24A4106, 24B4191, 24B4192, 24E4133, 24I4315, 24J4136, 24J4347; 07 7058/10643351000076/23G4430, 23G4168. Manufactured between July 31, 2023 and February 28, 2025.
Devices named in this recall
7 devices in the FDA device registry whose identifier appears in the recall's code information.
- SAFE-T-FILL® 07 6011Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 6013Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 7051Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 7052Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 7053Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 7056Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
- SAFE-T-FILL® 07 7058Ram Scientific, Inc · Tubes, vials, systems, serum separators, blood collection1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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