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.
Read the official notice →- Date
- 2024-02-21
- Country
- United States
- Brand
- Zimmer Surgical
- Product
- 3:1 Dermacarrier, Model Number 00219501300, skin graft carrier
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution including in the states of CA, DE, FL,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2026-07-08
USZimmer 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…
FDA · DeviceZimmer Surgical IncWorldwide distribution - US Nationwide and the countries of Canada and EMEA.Official notice →- 2026-02-04
- US
Zimmer 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 → - 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
- 2024-02-21
- US
Quidel Corporation recalls The Sofia 2 Flu + SARS Antigen FIA employs immunofluorescence technology in a sandwich design that is used with Sofia 2 to detect…
One lot of the Sofia 2 Flu + SARS Antigen FIA (Lot 709083) was labelled with incorrect expiration dates. The kits contain pouched cassettes labeled with an expiration date of May 31, 2025, however the correct…
FDA · DeviceQuidel CorporationUS Nationwide distribution in the states of FL, TN, IL, LA, NY, IN.Official notice → - US
Stryker, Inc. recalls Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
FDA · DeviceStryker, Inc.US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH,…Official notice → - US
SEDECAL SA recalls MobileDiagnost wDR, Model numbers 712001, 712002, 712004, 712006, and 712007
While cleaning or disinfecting the system, if the process is not followed as described in the manual and excessive liquid is used or sprayed directly on the system, it could cause a short circuit of the fine…
FDA · DeviceSEDECAL SAUS Nationwide distribution. There was government distribution but no military…Official notice → - US
Maquet Medical Systems USA recalls BEQ-HLS 7050 USA, HLS Set Advanced 7.0, Product Code/Part Number 70106.9078. Used with the CARDIOHELP heart-lung machine.
The Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis, or infection.
- US
Microbiologics Inc recalls Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
The negative control was contaminated with one of the positive control pathogens (Norovirus). This would result in users getting a positive call for Norovirus when running the negative control.
FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of AL, AZ, CA, CO, CT, DE, FL, GA,…Official notice → - US
Abiomed, Inc. recalls Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella…
New warnings are being added to the Instructions for Use for all affected products to reduce the possibility of fibers being drawn into the Impella, which may result in low flow of the device.
FDA · DeviceAbiomed, Inc.Worldwide distribution - US Nationwide and the countries of AU, CA, DE, FR,…Official notice →