Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
225 recalls match · Clear filters · Checked 12 minutes ago
United States
CanadaLIFECODES LSA Class II
Werfen has identified that two beads within the LIFECODES LSA class II assay kit(s) may present different DQB1 specificities than previously understood: • Bead 42 /…Glidesheath Slender® Introducer Sheath
Through post-market surveillance, we have received complaints for the guidewire not being able to pass through the needle.AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator
Complaint review identified a prior manufacturing process update that may cause erroneous overpressure alerts under certain conditions, potentially leading to loss of…Zimmer, Inc. recalls Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral…
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.Intuitive Surgical, Inc. recalls Da Vinci ASSY
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent…Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US…
Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process.GE Medical Systems, LLC recalls Giraffe OmniBed and 2 more products
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device.Arrow International, LLC recalls PARACENTESIS KIT and 34 more products
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets.A.T.S® 4000 TS Tourniquet Systems Single and Dual Hose with CPC Connectors
Zimmer Biomet is conducting a medical device recall for A.T.S® 4000 TS Tourniquet Systems Single and Dual Hose with CPC Connectors.Penumbra System RED 68 Reperfusion Catheter
Penumbra has identified an issue in the lots of RED 68 specified in this notification which may result in potential fracture of the device.Atellica CH Enzymatic Hemoglobin A1c (A1c_E) assay
Siemens Healthineers has confirmed, through internal investigation of customer complaints, the potential for intermittent well-to-well bias affecting the A1c_E/A1c_H…HALYARD* PUREZERO* Ultraviolet* Nitrile Exam Gloves
The issue surrounding this field action is related to not meeting the minimum breakthrough time of 30 minutes for n-Heptane required for European Type B performance per…Fresenius Medical Care Holdings, Inc. recalls Bicarby" Dialysate
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of…Sagemax Bioceramics, Inc. recalls NexxZr T Multi A3.5 W98-16mm
Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's…Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and HBV Quant Assay Software
This notification is to inform Panther and Panther Fusion users that assay installer (version 2.0.0.9) including the Aptima HIV Quant Dx Assay, HCV Quant Dx Assay, and…GE Medical Systems Information Technologies Inc recalls CASE v7.0 Cardiac Testing System Model no. 3031234-001 Product Code SU3
Electrical sparking may occur at the printer head.GE Medical Systems China Co., Ltd. recalls MAC 5 A4 Resting ECG Analysis System 855001-001
Software in development inadvertently made available for customer use.Kayserbetten GMBH & Co. KG recalls Pediatric care bed
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an…Stryker Corporation recalls Neptune Smart Docking Station
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior…Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set and 1 more products
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Renpure Tea Tree & Rosemary Scalp Rebalancing Shampoo & Conditioner recalled due to microbial contamination
These lot codes have elevated microbial levels including aerobic bacteria count, yeast/mold count and Burkholderia cepacia complex which may cause irritation and…Giraffe™ OmniBed™ Carestation™
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device.IceMan CLASSIC3â„¢
Complaints received reporting a consistent failure mode described as a broken connector on IceMan CLASSICâ„¢ cube unit.A little guidance
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