Manufacturer
464 recalls in our database name Medline Industries, LP as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Pending LLM rewrite. Source: FDA_DEVICE Z-2429-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2481-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2427-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2485-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2421-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2441-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2447-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2501-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2498-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2486-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2434-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2497-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2484-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2235-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2232-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2234-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2231-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2260-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2233-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2237-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2236-2026.
Medline Industries is recalling Namic Preceptor Manifold extravascular blood pressure transducers due to the presence of particulate matter within the fluid path. The recall affects 6,390 units distributed nationwide in the US and internationally.
Medline is recalling 107 medical convenience kits containing Namic Manifold (TAVI) due to particulate found in the fluid path. The kits were distributed nationwide and internationally.
Medline Industries is recalling cardiac medical convenience kits containing Namic Manifolds due to the presence of particulate matter within the fluid path. The affected kits were distributed nationwide and internationally.
Medline Industries is recalling the Namic Angiographic Manifold (Product Number 64038402) because particulate matter has been found in the fluid path. This medical device is used in cardiopulmonary bypass procedures.