Zimmer Surgical Inc recalls Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors Model/Catalog Number:…
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find…
Read the official notice →- Date
- 2026-07-08
- Country
- United States
- Brand
- Zimmer Surgical
- Product
- Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Single Hose with CPC Connectors Model/Catalog Number:…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of Canada and EMEA.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Zimmer Surgical recalls
- 2026-02-04
USZimmer Surgical Inc recalls Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version:…
Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.
FDA · DeviceZimmer Surgical IncInternational distribution to the countries of Canada and EMEA only.Official notice →- 2025-12-24
- US
Zimmer Surgical Inc recalls Zimmer Air Dermatome, Model/Catalog Number: 00880100100
The devices may have a misaligned thickness control bar.
FDA · DeviceZimmer Surgical IncDistribution regions: USA, Hong Kong, Thailand, Japan, Korea, Australia,…Official notice → - 2024-02-21
- US
Zimmer Surgical Inc recalls 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
Due to manufacturing issue, the product is labeled as 3:1 ratio, but the ridge pattern is a 1.5:1 ratio. The problem may lead to minor tissue damage or additional unplanned graft if deemed necessary.
FDA · DeviceZimmer Surgical IncWorldwide - US Nationwide distribution including in the states of CA, DE, FL,…Official notice → - 2023-10-11
- US
Zimmer Surgical Inc recalls Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use with the dermatome handpiece which is a skin grafting instrument that…
Skin grafts thin and non-uniform when using the affected blades. The issue would be identified at the time of use and may result in the need for additional harvests to adequately cover the area
FDA · DeviceZimmer Surgical IncUS Nationwide Foreign: AUSTRALIA BRAZIL CHINA HONG KONG INDIA JAPAN MALAYSIA…Official notice →
Other drugs & medical recalls in the United States
- 2026-07-15
- US
BioMed Laboratories, LLC. recalls Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL…
Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
- US
ONESOURCE SPECIALTY PHARMA LIMITED recalls Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial, Rx Only, Manufactured by: OneSource Specialty, Pharma…
Failed Impurities/Degradation Specifications
- 2026-07-09
- US
WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Walmart.com by…
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a…
- 2026-07-08
- US
W L Gore & Associates, Inc. recalls GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes Puerto Rico) and…
Due to catheter separation
FDA · DeviceW L Gore & Associates, Inc.Worldwide - U.S. Nationwide distribution including in the states and…Official notice → - US
Masimo Corporation recalls Radius VSM ECG pre-connected Set, REF: 4842, 4695
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger alarms on normal heart rate patients, which may distract clinicians…
FDA · DeviceMasimo CorporationWorldwide - US Nationwide distribution in the states of OK, CA , MD , MA , NY…Official notice → - US
Laborie Medical Technologies Corp recalls Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM…
Under extended clinical use conditions (e.g., long duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof…
FDA · DeviceLaborie Medical Technologies CorpWorldwide distribution - US Nationwide and the countries of Argentina,…Official notice →