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Hollister Incorporated

Hollister Incorporated Recalls

All product recalls associated with Hollister Incorporated.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 2141–2160 of 37661 recalls

AnchorFast Guard Select Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

Centurion Infusion Catheter (Medline) – Mislabeling (2024)

Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.

Low

FDADec 23, 2024FL, IL, KS +4 more• MEDLINE INDUSTRIES, LP Northfield

Storyteller GXV Hilt (Storyteller) – Frame Structural Issue (2024)

Storyteller Overland, LLC (Storyteller Overland) is recalling certain 2023-2024 GXV HILT vehicles. The metal frames within the housing portion of the vehicle may be improperly grounded.

High

NHTSA

1...106 107108109 110...1884

Page 108 of 1884Next

Dec 23, 2024

Nationwide

• STORYTELLER OVERLAND

Medline Arterial Line Pack (Medline) – Mislabeling (2024)

Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.

Low

FDADec 23, 2024FL, IL, KS +4 more• MEDLINE INDUSTRIES, LP Northfield

Tesla Model X (Tesla) – Airbag Deployment Risk (2024)

Tesla, Inc. (Tesla) is recalling certain 2021-2025 Model S and Model X vehicles. The driver's air bag could tear during deployment. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 208, "Occupant Crash Protection" and 212, "Windshield Mounting."

Moderate

NHTSADec 23, 2024Nationwide• TESLA

AnchorFast SlimFit Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

CyberKnife Treatment System (Accuray) – Snap Ring Detachment (2024)

Snap rings may become partially or completed detached from the shafts within the internal mechanism. Uncontrolled rotation may occur on the left and right roll axes when the rings are removed or damaged.

Moderate

FDADec 23, 2024Nationwide• Accuray Incorporated

AnchorFast Oral Endotracheal Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

Lev5 Susceptibility Discs (Oxoid) – Mislabeling Risk (2024)

Mislabeling; Levofloxacin Antimicrobial susceptibility disc packaging may contain Norfloxacin Antimicrobial Susceptibility discs.

Low

FDADec 23, 2024CA, FL, MA +4 more• Oxoid Limited Wade Road Basingstoke United Kingdom

Storyteller Beast Mode (Storyteller) – Electrical Issue (2024)

Fire/Burn Risk

Storyteller Overland, LLC (Storyteller Overland) is recalling certain 2024 Beast Mode, Classic Mode, Stealth Mode, and Mystic Mode vehicles. An improperly torqued internal component may cause the secondary alternator to short circuit and overheat.

High

NHTSADec 23, 2024Nationwide• STORYTELLER OVERLAND

Astagraf XL 0.5mg (Astellas) – empty capsules risk (2024)

Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules

Class IHigh

FDADec 23, 2024Nationwide• Astellas Pharma US Inc.

Ultra Repair Cream (First Aid Beauty) – distribution error (2024)

CGMP Deviations; product intended for quarantine was inadvertently distributed

Class IIModerate

FDADec 23, 2024Nationwide• First Aid Beauty Ltd

Prograf 0.5mg (Astellas) – empty capsules risk (2024)

Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain empty capsules

Class IHigh

FDADec 23, 2024Nationwide• Astellas Pharma US Inc.

AnchorFast Guard Tube Fastener (Hollister) – Skin Barrier Wear Time (2024)

Hollister received reports of decreased skin barrier wear time which could can lead to tube migration

Moderate

FDADec 23, 2024Nationwide• Hollister Incorporated

Life 2000 Ventilation System (Baxter) – Battery Charger Alarm (2024)

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

Moderate

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation

Baxter Solution Set (Baxter) – Inverted Side Clamps (2024)

Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.

Moderate

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation

Altec AT200A (Altec) – Suspension Spring Defect (2024)

Altec Industries, Inc. (Altec) is recalling certain 2017-2024 Ford E350 van chassis equipped with a AT200A devices. The units mounted on certain Ford E350 van chassis with Gross Axle Weight Rating (GAWR) of 4050 and 4200 pounds, may fail at high loads due to a defect in the front axle.

Moderate

NHTSADec 20, 2024Nationwide• ALTEC

Life2000 Ventilation System (Baxter) – Battery Charger Alarm (2024)

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

Moderate

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation

AXIOS Stent Delivery System (Boston Scientific) – Outer Sheath Detachment (2024)

Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.

Moderate

FDADec 20, 2024Nationwide• Boston Scientific Corporation

Life2000 Ventilation System (Baxter) – Battery Charger Alarm (2024)

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

Moderate

FDADec 20, 2024Nationwide• Baxter Healthcare Corporation