Manufacturer
787 recalls in our database name MEDLINE INDUSTRIES, LP - Northfield 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.
Medline Industries is recalling one lot of Meridian ImmunoCard STAT! Crypto/Giardia Test Kits due to improper temperature storage. The affected lot was distributed nationwide.
Medline is recalling sterile water and normal saline bottles in procedure kits due to leaking seals that compromise sterility. Affected units were distributed to healthcare facilities in the United States, Panama, and Canada.
Medline is recalling procedure kits because the sterile water and saline bottles leak at the peel-foil seal. The recall affects 822 units distributed in the US, Panama, and Canada.
Medline Industries is recalling 159 procedure kits containing sterile water and saline bottles due to leaks at the peel-foil seal interface. The defect could compromise product sterility.
Medline is recalling 240 units of NON STERILE I&D KIT (Lot 23KDB283) distributed in the US, Panama, and Canada. The Sterile Water and Normal Saline bottles in the kits are leaking at the peel-foil interface, compromising sterility.
Medline Sterile Water and 0.9% Normal Saline bottles are recalled due to leaking at the bottle opening interface, which may compromise product sterility and safety for medical use.
Medline Sterile Water and 0.9% Normal Saline bottles may leak at the peel-foil seal, potentially compromising sterility. Units were distributed to the US, Panama, and Canada.
Medline procedure kits containing Sterile Water and Sterile 0.9% Normal Saline bottles are being recalled due to leaking at the seal interface. The defective bottles may compromise sterility, affecting procedure kits distributed nationwide and internationally.
Medline is recalling sterile water and 0.9% normal saline bottles used in procedure kits due to leaking at the peel-foil and bottle opening interface. The recall affects 2,220 units distributed in the US, Panama, and Canada.
Medline is recalling 5,200 procedure kits with sterile solution bottles that may leak at the seal, potentially compromising sterility. Affected units were distributed nationwide in the US, Panama, and Canada.
Medline Sterile 0.9% Normal Saline bottles are being recalled due to leaking at the peel-foil and bottle opening interface, which compromises product sterility. The recall affects approximately 2.5 million units distributed in the US, Panama, and Canada.
Medline Industries is recalling select sterile surgical convenience kits due to potential weak or open seals on breather pouches. Compromised seals could allow contamination of sterile supplies.
Medline Industries is recalling 3,205 sterile surgical convenience kits with potential weak or open seals on their breather pouches. Seal defects may allow contamination and loss of product sterility.
Medline is recalling 9,216 surgical convenience kits due to weak or open seals on breather pouches that could compromise sterility. Affected kits include ENT, T&A, and other procedure packs distributed nationwide and internationally.
Medline Industries is recalling 4,094 surgical convenience kits due to potential open or weak seals on breather pouches that could compromise sterility.
Medline Industries is recalling certain sterile convenience kits due to potential weak or open seals on breather pouches used for packaging. Compromised seals could affect product sterility.
Medline is recalling 3,909 ophthalmic surgical convenience kits due to potentially weak or open seals on breather pouches that maintain product sterility. The seal defect could compromise the sterile contents during storage or use.
Medline has recalled two models of convenience kits due to potential open or weak seals on packaging breather pouches. Approximately 530 units distributed worldwide may be affected.
Medline Industries is recalling 28,127 sterile convenience kits due to potential open or weak seals on breather pouches used for packaging. The defect could compromise product sterility.
Medline is recalling 21,935 sterile convenience kits used for obstetrical procedures due to potential open or weak seals on breather pouches that could compromise product sterility. The kits were distributed nationwide and internationally.
Medline is recalling Rhinoplasty Convenience Kits (Model DYNJ84116A, Lot 24IBH580) due to potential open or weak seals on breather pouches. Compromised seals could affect package sterility, though no illnesses have been reported.
Medline is recalling 4,022 sterile procedure kits due to potential open or weak seals on breather pouches that could compromise sterility.
Medline is recalling sterile convenience kits used for various procedures because breather pouches may have open or weak seals, which could compromise sterility during storage or transport.
Medline is recalling certain sterile convenience kits packaged with breather pouches that may have open or weak seals. Approximately 14,760 units were distributed worldwide.
Medline is recalling 56 Rhinoplasty Packs due to weak or open seals on breather pouches. The packaging defect may compromise sterility of the surgical kits.