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MEDLINE INDUSTRIES, LP - Northfield Recalls

822 recalls on record · December 29, 2021 to October 1, 2025 · Drugs, Medical Devices

Recalls by year

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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

June 1, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954
Hazard: Product was shipped from a Medline warehouse to a customer at room temperature instead of refrigerated (ice). If affected product is used, the results from this impacted Calcium reagent will not be provided due to probable Quality Control failure. A delay in diagnosis may be experienced with repeat testing resulting in patient (customer) inconvenience, pain, and cost of the repeat blood draw and testing. All HII1220001954 product shipped/stored at a Medline branch between July 2021 and August 2021 in the identified lots were incorrectly stored and shipped. Six (6) boxes have been shipped to end users at room temperature instead of refrigerated (ice). Five (5) boxes are on hold at a Medline warehouse.
April 20, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Hazard: The mask cuff may disconnect from the device's breathing tube.
April 20, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-6
Hazard: The product was stored incorrectly due to improper storage controls which may lead to delayed results.
April 20, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Hazard: Product was improperly store which may cause a delay in results.
April 13, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV
Hazard: Sterility failure of the exterior of the syringe which may impact the device's ability to be laid on a sterile field.
March 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Hazard: Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.
March 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immun
Hazard: The product was incorrectly shipped at room temperature rather than refrigerated.
March 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Michels Transport Medium, 20ML Prefilled Cont
Hazard: Product stored incorrectly in temperature controlled setting instead of refrigeration.
February 16, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CURAD REUSABLE GEL HOT/COLD PACK
Hazard: The product contains natural rubber latex but the label states that it does not.
February 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls HARDY DIAGNOSTICS CatScreen, 25dsk/vial
Hazard: Product stored incorrectly in temperature controlled setting instead of refrigeration.
February 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Premier Rotaclone, Rx only
Hazard: Product stored incorrectly in temperature controlled setting instead of refrigeration.
December 29, 2021Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
Hazard: Affected product was shipped from the warehouse at room temperature instead of the required refrigerated environment.