Manufacturer

MEDLINE INDUSTRIES, LP - Northfield

822 recalls in our database name MEDLINE INDUSTRIES, LP - Northfield as the manufacturing or recalling firm.

What the numbers show

Total: 822
Critical: 9
Severe: 66
Most recent: 2025-10-01

Of the 822 recalls from MEDLINE INDUSTRIES, LP - Northfield we have scored against our rubric, 9 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 66 (8%) are Severe.

Which agencies issued them

About this listing

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.

801–822 of 822

HighFDA (Devices)·Z-1857-2022·2022-10-05
Medline ClearPro Trach T-Piece Suction Catheter May Separate at Connector
Medline is recalling 136,080 ClearPro Trach T-Piece Closed Suction Catheters because the suction catheter can come apart from the connector during patient suctioning.
Product
MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14; b. TRACH T-PIECE, 14 Fr, Item Number/REF: DYNCPTP14T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1855-2022·2022-10-05
Medline ClearPro Suction Catheter Connector May Separate During Use
Medline ClearPro closed suction catheters may have a connector that separates from the device during patient suctioning. The malfunction affects 65,320 units distributed nationwide and internationally.
Product
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. ET LENGTH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12; b. ET LENGTH DOUBLE SWIVEL, 14 Fr, Item Number/R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1856-2022·2022-10-05
Medline suction catheters recalled due to connector separation risk
Medline ClearPro Trach Double Swivel Closed Suction Catheters may have the green connector separate from the device during patient suctioning. The recall affects 34,920 units distributed nationwide and internationally.
Product
MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner cartons per Case (CS). Labeled as follows: a. TRACH DOUBLE SWIVEL, 12 Fr, Item Number/REF: DYNCPDS12T b. TRACH DOUBLE SWIVEL, 14 Fr, Item Number/REF:
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1493-2022·2022-08-10
Medline germicidal bleach wipes recalled due to stability failure
Medline Micro-Kill Germicidal Bleach Wipes are being recalled nationwide due to stability failure affecting approximately 6.1 million wipes across multiple lot numbers.
Product
MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES, Model numbers MSC351420AN, MSC351420ANH, MSC351420ANZ, MSC351430A, MSC351430AZ
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1287-2022·2022-07-06
Medline Pill Splitters recalled for unhinged lid exposing sharp blade
Medline is recalling over 840,000 pill splitters due to a defect where the product lid can come unhinged, exposing a sharp blade and posing a laceration risk.
Product
Medline Pill Splitters; 1 each/box; 144 boxes/carton
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1217-2022·2022-06-08
MEDLINE Enzymatic Cleaning Sponges Recalled Due to Microbial Contamination
MEDLINE Polyurethane Foam Enzymatic Cleaning Sponges (REF DYK1000TSE) are being recalled due to microbial contamination identified on certain lots. The affected product was distributed in the US and Panama.
Product
MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1219-2022·2022-06-08
MEDLINE Polyurethane Bedside Cleaning Kits Recalled Due to Microbial Contamination
MEDLINE is recalling certain lots of its Polyurethane Bedside Cleaning Kits due to confirmed microbial contamination on the foam sponge. The kits were distributed in the US and Panama.
Product
MEDLINE Polyurethane Bedside Cleaning Kit, REF DYK500FSAW
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1218-2022·2022-06-08
MEDLINE Polyurethane Foam Bedside Cleaning Kit Recalled for Microbial Contamination
MEDLINE has recalled its Polyurethane Foam Bedside Cleaning Kit (REF DYK500FS) in the United States and Panama after sporadic reports of discoloration. The discoloration has been identified as microbial contamination.
Product
MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK500FS
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1220-2022·2022-06-08
Medline Polyurethane Foam Bedside Cleaning Kit recalled for microbial contamination
Medline Industries recalls Polyurethane Foam Bedside Cleaning Kits due to sporadic reports of discoloration on foam sponges caused by microbial contamination. The recall affects 22,765 boxes distributed in the US and Panama.
Product
MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK215FS
Category
Medical Device
Distribution
0 states
ModerateFDA (Devices)·Z-1221-2022·2022-06-08
MEDLINE Polyurethane Foam Bedside Cleaning Kit Recalled for Microbial Contamination
MEDLINE has recalled certain lots of its Polyurethane Foam Bedside Cleaning Kit due to microbial contamination detected on the foam sponge. Sporadic reports of discoloration were identified as contamination.
Product
MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK100FS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1140-2022·2022-06-01
Medical Calcium Reagent Shipped Without Required Refrigeration; QC Failure Risk
A medical lab reagent (ABX Pentra Calcium AS CP) was shipped at room temperature instead of refrigerated, causing probable quality control failure. Affected patients may experience diagnostic delays and require repeat testing.
Product
ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954
Category
Medical Device
Distribution
1 state
HighFDA (Devices)·Z-0941-2022·2022-04-20
Medline Laryngeal Masks recalled due to potential cuff disconnection
Medline Industries is recalling approximately 8,990 cases of Standard PVC Laryngeal Masks distributed nationwide because the mask cuff may disconnect from the breathing tube.
Product
Medline Standard PVC Laryngeal Masks, 1 device per pouch, 5 each pouches per box
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0933-2022·2022-04-20
Medical Device Linearity Standards Recalled Due to Improper Storage Controls
Medline Industries is recalling Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards due to improper storage controls that may affect test result timing. The recall affects 10 boxes distributed to healthcare facilities in six states.
Product
Stanbio TDM/Beta-Hydroxybutyrate Linearity Standards, packaged in boxes containing Levels 1-6, 1 x 4 mL each, REF 2450-604, Medline catalog number S-O2450604, IVD.
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-0932-2022·2022-04-20
Hydroxybutyrate Test Kits Recalled Due to Improper Storage
Medline's Hydroxybutyrate LiquiColor Tests are recalled due to improper storage that may cause delayed test results. The recall affects 45 units distributed across 16 U.S. states.
Product
Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Category
Medical Device
Distribution
16 states
HighFDA (Devices)·Z-0898-2022·2022-04-13
Medline Excelsior Medical Sterile Saline Flush Syringes Recalled for Sterility Failure
Medline Industries is recalling 7,800 Excelsior Medical 10mL Sterile Field Saline Flush syringes due to sterility failure of the exterior syringe surface, which may prevent the product from being safely used on a sterile field.
Product
Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV Flush Only, Contents of Package may be dropped on a Sterile Field, 1 syringe/pouch, 35 pouches/box, 8 boxes/case.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0696-2022·2022-03-09
MEDLINE Micro-Kill Bleach Germicidal Wipes Recall: Out-of-Specification Sodium Hypochlorite
MEDLINE recalls Micro-Kill Bleach Germicidal Wipes due to out-of-specification low levels of sodium hypochlorite, the active disinfecting ingredient. Affected batches may have reduced effectiveness.
Product
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0678-2022·2022-03-02
ImmunoCard STAT Rotavirus diagnostic tests recalled for improper storage temperature
Meridian BioscienceImmunoCard STAT! Rotavirus tests were shipped at room temperature instead of refrigerated, which may affect their reliability.
Product
meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immunoassay is a rapid in vitro qualitative procedure for the detection of rotavirus antigen in human stool. The test can be used to aid in the diagnosis of rotaviru
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-0656-2022·2022-03-02
Medline Michels Transport Medium Recalled for Improper Storage Conditions
Medline is recalling 2,816 Michels Transport Medium prefilled containers due to improper storage in a temperature-controlled setting instead of refrigeration.
Product
Michels Transport Medium, 20ML Prefilled Cont
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0633-2022·2022-02-16
CURAD Reusable Gel Hot/Cold Pack Contains Undisclosed Natural Rubber Latex
Medline Industries is recalling 494,273 CURAD Reusable Gel Hot/Cold Packs because the product contains natural rubber latex that is not disclosed on the label. Consumers with latex allergies face risk of allergic reaction.
Product
CURAD REUSABLE GEL HOT/COLD PACK
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0552-2022·2022-02-09
Premier Rotaclone Medical Device Recalled Due to Improper Storage Conditions
Medline Industries is recalling 34 units of the Premier Rotaclone (Lot 696004N116) due to improper storage in temperature-controlled settings instead of required refrigeration. This may affect device performance or safety.
Product
Premier Rotaclone, Rx only
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0554-2022·2022-02-09
HARDY DIAGNOSTICS CatScreen diagnostic kit recalled due to improper storage
HARDY DIAGNOSTICS CatScreen test kits (Model HADZ110) are recalled because units were stored in temperature-controlled settings instead of refrigeration. Improper storage may compromise product effectiveness.
Product
HARDY DIAGNOSTICS CatScreen, 25dsk/vial
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0404-2022·2021-12-29
Stanbio TDM/B-Hydroxybutyrate Controls Recalled Due to Improper Storage Temperature
Medline Industries is recalling Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls due to improper storage conditions. The product was shipped at room temperature instead of the required refrigerated environment.
Product
Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
Category
Medical Device
Distribution
Distributed nationwide