Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare, Catalog No. 7202
During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may result.
Read the official notice →- Date
- 2022-07-27
- Country
- United States
- Brand
- Hobbs Medical
- Product
- Hobbs Medical Polypectomy Snare, Catalog No. 7202
- Classification
- Class II
- Units
- Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Hobbs Medical recalls
- 2024-11-27
USHobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the…
FDA · DeviceHobbs Medical, Inc.Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN,…Official notice →- 2022-10-19
- US
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9/28/2020, expiration dates between 2022-11-01 and…
FDA · DeviceHobbs Medical, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Austria,…Official notice → - 2022-03-09
- US
Hobbs Medical, Inc. recalls Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush…
The labeling for the Microbiology Brush identifies the device as a Bronchial Microbiology Brush. The device is only cleared for gastrointestinal use and is not cleared for bronchial use.
Other drugs & medical recalls in the United States
- 2022-07-27
- US
Aesculap Implant Systems LLC recalls ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with EnduRo Total Knee System. instrument used during orthopedic…
Nonfunctional key due to the potential for damage to the key pins cause by force of use during assembly of the tibia locking ring.
FDA · DeviceAesculap Implant Systems LLCUS Nationwide distribution in the states of AL, AZ, CA, CO, ID, IL, LA, MA,…Official notice → - US
R & D Systems, Inc. recalls Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations…
The Instructions for Use (IFU, Part Number 750095) provided with the affected lots by the firm contains an error associated with product s CE marking. The CE mark contained in the IFU is followed by the Notified Body…
FDA · DeviceR & D Systems, Inc.Worldwide distribution - US Nationwide distribution in the states of FL, MN,…Official notice → - US
GE Healthcare, LLC recalls GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number…
There is a potential reversal of the O2 and air cylinder pressure transducer connections.
FDA · DeviceGE Healthcare, LLCWorldwide Distribution. US nationwide, Australia, Austria, Belgium, Bolivia,…Official notice → - US
SONEX HEALTH LLC recalls SX-One MicroKnife
Potential of dull blade
FDA · DeviceSONEX HEALTH LLCUS Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, ID, IN,…Official notice → - US
Stryker Neurovascular recalls Trevo Trak 21 Microcatheter, REF: 90338. TREVO NXT 3X32+TRAK21 2-PACK - CE, REF: 91412; TREVO NXT 4X28+TRAK21 2-PACK - CE, REF: 91413;…
Microcatheter product label on the carton is missing the microcatheter product drawing/illustration.
FDA · DeviceStryker NeurovascularWorldwide distribution - US Nationwide distribution in the states of CA, OR,…Official notice → - US
Loud Muscle Science recalls Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
FDA · DrugLoud Muscle ScienceThe product was distributed nationwide in the USA and Canada.Official notice →