Hobbs 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…
Read the official notice →- Date
- 2024-11-27
- Country
- United States
- Brand
- Hobbs Medical
- Product
- Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-10-19
USHobbs 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 →- 2022-07-27
- US
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.
FDA · DeviceHobbs Medical, Inc.Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.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
- 2024-11-27
- US
ICU Medical, Inc. recalls Allegedly counterfeit batteries manufactured by CSB batteries being used with Plum Infusion Systems: Plum 360" Infusion System, Pump List…
ICU Medical has received reports of allegedly counterfeit CSB batteries being used with Plum Infusion Systems. While these non-OEM batteries are visually similar to the Plum batteries supplied by ICU Medical, they are…
FDA · DeviceICU Medical, Inc.Worldwide distribution: US (nationwide) including Puerto Rico and OUS…Official notice → - US
Caire, Inc. recalls CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Potential failure of affected units to recharge the battery of the oxygen concentrators.
FDA · DeviceCaire, Inc.Worldwide distribution - US Nationwide, including PR and the countries of…Official notice → - US
Biomet, Inc. recalls JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to…
FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of Australia, Brazil,…Official notice → - US
Bard Peripheral Vascular Inc recalls Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT 12G X 10 CM, REF: MQK1210; BARD MARQUEE 12G X 10 CM, REF:…
Disposable biopsy instruments were potentially manufactured missing the backend notch retention feature on the needle that results in inadequate securing of the needle inside the device, which could lead to needle…
FDA · DeviceBard Peripheral Vascular IncWorldwide - US Nationwide including in the states of WA, LA, MN, PA, UT, SC,…Official notice → - US
Smiths Medical ASD, Inc. recalls smiths medical CADD-Solis Li-ion Rechargeable Battery Packs AC adapter, Model Number REF 21-0270-25, for use with the CADD-Solis…
The adapter input plug can become damaged or broken. If the input plug is damaged, the metal contacts to the body of the AC adapter may be exposed or one or more of the AC mains prongs may separate from the input plug.
- US
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using…
FDA · DeviceBaxter Healthcare CorporationWorldwide Distribution (US Nationwide distribution)Official notice →