TELEFLEX LLC recalls Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton)…
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
Read the official notice →- Date
- 2026-07-08
- Country
- United States
- Brand
- Teleflex
- Product
- Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips (Cotton)…
- Classification
- Class II
- Units
- Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Teleflex recalls
- 2023-07-12
USTELEFLEX LLC recalls Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
- 2023-07-05
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TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170085
Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
- 2023-06-07
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TELEFLEX LLC recalls Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that require vessel or…
Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step…
- 2023-05-24
- US
TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tracts of femoral…
The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
- 2023-02-01
- US
TELEFLEX LLC recalls Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b. Endotracheal Tube…
Potential for pilot balloon non-inflation or cuff non-deflation.
FDA · DeviceTELEFLEX LLCWorldwide - US Nationwide distribution including in the states of AL, AR, AZ,…Official notice → - 2023-01-04
- US
TELEFLEX LLC recalls Pilling Wecksorb Cylindrical Sponges
Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
Other drugs & medical recalls in the United States
- 2026-07-08
- US
Medela Inc recalls Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086 Software Version: N/A…
May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery of enteral nutritional fluids or oral medication.
FDA · DeviceMedela IncUS distribution to the following states: AZ, CA, CO, FL, HI, IL, IN, MD, MI,…Official notice → - US
Accuray Incorporated recalls Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room…
FDA · DeviceAccuray IncorporatedWorldwide - US Nationwide and and the countries of Australia, Austria,…Official notice → - US
Siemens Medical Solutions USA, Inc recalls ARTIS icono floor. Model Number: 11327700.
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
- US
Baxter Healthcare Corporation recalls Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back…
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating…
FDA · DeviceBaxter Healthcare CorporationWorldwide - US Nationwide distribution in the states of Minnesota, Maryland,…Official notice → - US
Boston Scientific Corporation recalls CRE Pro Wireguided 12-15mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
FDA · DeviceBoston Scientific CorporationWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
FDA · DeviceHamilton Medical AGWorldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA,…Official notice →