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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

SAFE-T-FILL Blood Collection Tubes Recalled for False Positive Lead Results

Agency Publication Date: October 27, 2025
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Summary

Anatomy Supply Partners, LLC has recalled 4,272,858 RAM SAFE-T-FILL Micro Capillary Blood Collection tubes because they can cause false positive results for lead levels when used with Magellan Diagnostics LeadCare Testing Systems. This recall affects tubes manufactured between July 31, 2023, and February 28, 2025, in various sizes and configurations including purple-cap models with EDTA additives. No injuries or incidents have been reported to date, but the diagnostic error can lead to delayed results and unnecessary medical testing.

Risk

The recalled blood collection tubes interfere with specific lead testing equipment, producing falsely high lead readings. This poses a risk of incorrect diagnoses, which can lead to unnecessary follow-up procedures or delays in identifying and treating actual lead exposure.

What You Should Do

  1. This recall affects multiple models of RAM SAFE-T-FILL Micro Capillary Blood Collection tubes, including the 125 µL, 150 µL, 200 µL, and 300 µL sizes prepared with Dipotassium EDTA.
  2. Check the model number and lot number printed on the product packaging or device label to see if your supply is affected. Affected model numbers include 07 6011, 07 6013, 07 7051, 07 7052, 07 7053, 07 7056, 07 7058, and 06 0910. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled collection tubes immediately for any lead testing procedures.
  4. Contact Anatomy Supply Partners, LLC or your medical supply distributor to arrange for the return, replacement, or correction of your inventory.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding this recall.

Your Remedy Options

📋Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (125 µL)
Variants: 125 µL, Purple Cap, Dipotassium EDTA
Model / REF:
07 6011
Lot Numbers:
23H4110
23I4017
23I4051
23J4031
23K4058
23K4059
23L4082
24A4103
24B4186
24B4187
24D4015
24E4138
24E4139
24H4121
24I4317
24I4328
24J4041
24J4137
24J4138
24J4233
24J4316
24J4348
UDI:
10643351000014
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025

Prepared with Dipotassium EDTA Purple.

Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (125 µL, Self-sealing Cap)
Variants: 125 µL, Self-sealing Cap, Purple, Dipotassium EDTA
Model / REF:
07 6013
Lot Numbers:
23H4111
23I4018
24B4188
24H4125
25B4099
UDI:
10643351000021
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (200 µL)
Variants: 200 µL, Purple, Dipotassium EDTA
Model / REF:
07 7051
Lot Numbers:
23H4157
23I4020
23I4374
23J4033
23K4060
23L4083
24A4104
24B4190
24D4016
24E4140
24F4053
24I4321
24J4043
24J4139
24J4237
24L4001
25B4107
UDI:
10643351000038
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (150 µL)
Variants: 150 µL, Purple, Dipotassium EDTA
Model / REF:
07 7052
Lot Numbers:
23H4113
23I4021
23J4034
24A4105
24D4017
24F4052
24H4126
24I4323
24J4042
24J4140
24J4338
24J4355
25B4108
UDI:
10643351000045
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (300 µL)
Variants: 300 µL, Purple, Dipotassium EDTA
Model / REF:
07 7053
Lot Numbers:
23I4022
23J4035
23L4084
24D4018
24E4132
24F4192
25B4106
UDI:
10643351000052
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (200 µL)
Variants: 200 µL, Purple, Dipotassium EDTA
Model / REF:
07 7056
Lot Numbers:
24A4106
24B4191
24B4192
24E4133
24I4315
24J4136
24J4347
UDI:
10643351000069
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL Micro Capillary Blood Collection Tube (200 µL, Flat Bottom)
Variants: 200 µL, Flat Bottom, Purple, Dipotassium EDTA
Model / REF:
07 7058
Lot Numbers:
23G4430
23G4168
UDI:
10643351000076
Date Ranges: Manufactured between July 31, 2023 and February 28, 2025
Product: SAFE-T-FILL End-to-End Capillary Tubes (30 µL)
Variants: 30 µL, Plastic, EDTA Dipotassium
Model / REF:
06 0910

Quantity affects overall totals but lot information not specifically listed in main code block.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97551
Status: Active
Manufacturer: ASP Global, LLC. dba Anatomy Supply Partners, LLC.
Sold By: ASP Global, LLC; Anatomy Supply Partners, LLC; Authorized medical distributors
Manufactured In: United States
Units Affected: 4,272,858
Distributed To: Alaska, Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New York, Ohio, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.