Has Medline Industries, LP had other FDA recalls or enforcement actions?

Yes. Argus HQ has recorded 293 total FDA actions tied to Medline Industries, LP, including 293 recalls and 0 warning letters.

What is the current status of this recall?

Status as recorded by FDA: Ongoing.

Where can I verify this recall directly with FDA?

The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

FDA Class I Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating… by Medline Industries, LP

Key facts

Recalling firm	Medline Industries, LP
Manufacturer	Not disclosed in the FDA record.
Brand name	Not disclosed in the FDA record.
Product description	Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
Classification	Class I
Recall number	Z-1723-2026
Report date	Not disclosed in the FDA record.
Status	Ongoing
Reason for recall	Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

In short: Medline Industries, LP recalled Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596 on 2026-04-15. FDA classified this action as a Class I recall (recall number Z-1723-2026). Reason for recall: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.. Recall status: Ongoing. This is a device-category FDA recall record.

What this classification means

FDA classifies a recall as Class I when there is a reasonable probability that using the recalled product, or being exposed to it, will cause serious adverse health consequences or death. Class I is FDA's most serious recall classification. In this case, the recalling firm is Medline Industries, LP and the affected product is described in FDA's record as: Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596. FDA's stated reason for the recall is: Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.. The recall is tracked under FDA recall number Z-1723-2026 and carries a status of Ongoing as of the most recent FDA enforcement report. This classification reflects FDA's assessment of the product defect described above, not a prediction about any specific patient outcome. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do. Recall status can change while FDA and the recalling firm continue corrective actions, so checking the firm's own notice for the most current guidance is recommended.

What consumers should do

Because FDA has assigned this recall its highest severity classification, anyone who has this product should stop using it immediately, regardless of whether a problem has been noticed yet. Specifically, check whether the product in your possession matches the description on file with FDA -- Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596 -- and the recall number Z-1723-2026. If it matches, stop using or distributing it and contact Medline Industries, LP or the point of purchase for return or replacement instructions. Retailers and distributors holding affected inventory should quarantine it and follow the firm's written recall notice. FDA maintains a public enforcement report database so that consumers, physicians, and purchasers can look up the exact product identifiers involved before deciding what to do.

Medline Industries, LP’s FDA history

Argus HQ has recorded 293 total FDA actions tied to Medline Industries, LP: 0 warning letters, 293 recalls, 0 approval records, and 0 Form 483 inspection citations.

Frequently asked questions

Has Medline Industries, LP had other FDA recalls or enforcement actions?: Yes. Argus HQ has recorded 293 total FDA actions tied to Medline Industries, LP, including 293 recalls and 0 warning letters.
What is the FDA recall number for this event?: FDA recall number Z-1723-2026.
What is the current status of this recall?: Status as recorded by FDA: Ongoing.
Where can I verify this recall directly with FDA?: The verbatim FDA record is the source of truth for every recall Argus HQ tracks — always confirm against fda.gov before acting.

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Full FDA history for Medline Industries, LP

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). FDA Class I Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating… by Medline Industries, LP — Recall Details. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/recall/fda-recall-medline-industries-lp-z-1723-2026

MLA

"FDA Class I Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating… by Medline Industries, LP — Recall Details." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/recall/fda-recall-medline-industries-lp-z-1723-2026.

Chicago

Argus HQ Research. "FDA Class I Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating… by Medline Industries, LP — Recall Details." Digital Empire Holdings LLC. Accessed September 7, 2026. https://argushq.ai/recall/fda-recall-medline-industries-lp-z-1723-2026.

BibTeX

@misc{argushq_argushq_ai_recall_fda_recall_medline_industries_lp_z_1723_2026_2026,
  title = {FDA Class I Recall: Medline medical convenience kits, containing NAMIC Angiographic Rotating… by Medline Industries, LP — Recall Details},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/recall/fda-recall-medline-industries-lp-z-1723-2026},
  note = {Accessed: September 7, 2026}
}

Source: FDA.gov — Recalls ↗