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Medline Industries Inc

Medline Industries Inc Recalls

All product recalls associated with Medline Industries Inc.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 32721–32740 of 37665 recalls

Medline Industries Inc: Medline Latex Free Mom/Baby Admit Kit - LF; a single pati...

The latex free labor & delivery packs contain a latex Nuk pacifier. The pacifier is packaged separately and offers no risk of exposure of latex particles to other components of the pack.

FDAAug 4, 2008Nationwide• Medline Industries Inc

Medline Industries Inc: Medline Latex Free C-Section CDS-LF and C-Section Supplem...

The latex free labor & delivery packs contain a latex Nuk pacifier. The pacifier is packaged separately and offers no risk of exposure of latex particles to other components of the pack.

FDAAug 4, 2008Nationwide• Medline Industries Inc

Medline Industries Inc: Medline Latex Free Labor & Delivery CDS-LF; a single pati...

The latex free labor & delivery packs contain a latex Nuk pacifier. The pacifier is packaged separately and offers no risk of exposure of latex particles to other components of the pack.

1...1635 163616371638 1639...1884

Page 1637 of 1884Next

FDAAug 4, 2008Nationwide• Medline Industries Inc

Immunodiagnostics Systems Inc: IDS 25-Hydroxy Vitamin D EIA Enzymeimmunoassay for the qu...

A small number of customers have experienced low absorbance values when using kits from this batch.

FDAAug 2, 2008Nationwide• Immunodiagnostics Systems Inc

King Systems Corp.: King Systems, Datex-Ohmeda, Universal Flex2 Breathing Cir...

The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.

FDAAug 1, 2008Nationwide• King Systems Corp.

King Systems Corp.: King Systems Universal Flex2 Breathing Circuit, Latex Fre...

The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.

FDAAug 1, 2008Nationwide• King Systems Corp.

King Systems Corp.: King Systems 72" Universal Flex2 Extension Kit, 50 per ca...

The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.

FDAAug 1, 2008Nationwide• King Systems Corp.

Sunquest Information Systems, Inc.: Sunquest Laboratory System. Software Version: Sunquest ...

While performing in-house testing for the Sunquest Laboratory System and under certain conditions, there have been instances in which an error that occurred at the database level or originated in the operating system (Cache)was not communicated or displayed in the Graphic User Interface (GUI) application so the activity continued. While this error was registered in the error log in the System U

FDAAug 1, 2008Nationwide• Sunquest Information Systems, Inc.

King Systems Corp.: King Systems 37" Universal Flex2 Extension Kit, 50 per ca...

The inner line may be severed or broken into two pieces, thus hindering the delivery of oxygen and anesthetics to the patient and possibly elevated patient carbon dioxide levels.

FDAAug 1, 2008Nationwide• King Systems Corp.

Baxter Bioscience: FloSeal Endoscopic Applicator , Product Code 1500181. Th...

The recall is being conducted as a precautionary measure due to potential discoloration of the FloSeal material noted in six (6) non-medical complaints during delivery by the Endoscopic Applicator.

FDAJul 31, 2008Nationwide• Baxter Bioscience

Vance Products Incorporated: Cook Urological Endoureterotomy Stent Set, 10Fr/13 cm, 6....

The bond may break where the two materials meet, resulting in separation of the stent.

FDAJul 31, 2008Nationwide• Vance Products Incorporated

Intelifuse Inc: InteliFUSE, Drill Bit, 1.50 mm, J-Latch, QTY: 1, REF: DB...

Manufacturing specification for drill bit was incorrect which, when used in conjunction with the drill guide, could cause the production of metal shavings.

FDAJul 30, 2008Nationwide• Intelifuse Inc

Intelifuse Inc: InteliFUSE, Drill Bit, 2.00 mm, J-Latch, QTY: 1, REF: DB...

Manufacturing specification for drill bit was incorrect which, when used in conjunction with the drill guide, could cause the production of metal shavings.

FDAJul 30, 2008Nationwide• Intelifuse Inc

Bio-Rad Laboratories: Kallestad (TM) Mouse Stomach/Kidney, catalog number 30443...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: Kallestad (TM) HEp-2 Cell Line Substrate. Product labele...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories

Wooden Toys (Earthentree) - Choking Risk (2008)

Choking Hazard

This recall involves a variety of wooden toys including egg shakers (maracas), pull toys, rattles, and trains. The toys are painted glossy red, orange, green, brown, yellow or natural wood.

CPSCJul 29, 2008Nationwide• Earthentree of Kirkland, Wash.

Bio-Rad Laboratories: Kallestad (TM) Mouse Kidney. Product labeled "BIO-RAD Ka...

The Homogeneous Positive control was released with a titer of 1:256 rather than the titer value of 1:128 reported on the QC Report Label included with each test kit.

FDAJul 29, 2008Nationwide• Bio-Rad Laboratories

Greiner Bio-One North America, Inc.: VACUETTE, 2 ml Lithium Heparin Venous Blood Collection Tu...

Labeling Error: Incorrect tube label reads "Z Serum Clot Activator" instead of "LH Lithium Heparin" tube. All other information on the tube label including color coding of tube was correct. Case and rack label information showed the correct information with 2 ml Lithium Heparin.

FDAJul 29, 2008AL, AK, AR +30 more• Greiner Bio-One North America, Inc.

Neurotherm, Inc.: NeuroTherm Simplicity III RF Electrode Model Number: R...

Distal tip may detach from the probe

FDAJul 28, 2008CO, FL, IL +5 more• Neurotherm, Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo II VR D284VRC, for ventricular pacing an...

Maximo II VR ICD, DR ICD and CRT-D inadvertently include the Capture Management algorithm (Atrial/Right Ventricular/Left Ventricular Capture management). The Capture management algorithm monitors daily pacing thresholds and may increase or decrease pacing amplitudes in response to patients' needs. Although the algorithm is operating correctly, it is not accessible to the clinician for reprogramm

FDAJul 25, 2008Nationwide• Medtronic Inc. Cardiac Rhythm Managment