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Medical Device
FDA DevicesClass II

OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG12...

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Jul 8, 2026Bard Access Systems, Inc.
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TU...

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Jul 8, 2026Medline Industries, LP
Food & Beverage
FDA FoodClass II

MorningStar Farms Hot & Spicy Sausage Patties, 100% Plant Protein Vegan Sausage ...

Potential contamination with plastic material

Jul 8, 2026MARS SNACKING
Pharmaceutical
FDA DrugsClass II

BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v ...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Medical Device
FDA DevicesClass II

CRE Wireguided 12-15mm 240cm

Potential sterile breach of the pouches in which devices are packaged.

Jul 8, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass II

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotto...

Due to out-of-specification, or potential out-of-specification, levels of endotoxins

Jul 8, 2026TELEFLEX LLC
wiseup - gant de protection multiusage
RappelConsovolontaire (san...

wiseup - gant de protection multiusage

non conforme aux normes europénnes

Jul 8, 2026wiseup
Pharmaceutical
FDA DrugsClass II

BD ChloraPrep Hi-Lite Orange, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v ...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
pas de marque. - herbes épices bbq
RappelConsovolontaire (san...

pas de marque. - herbes épices bbq

résidus de pesticides.

Jul 8, 2026pas de marque.
Pharmaceutical
FDA DrugsClass II

ChloraPrep FREPP, Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopr...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
Medical Device
FDA DevicesClass I

Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5...

External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or bolus delivery. The primary failure mode is pump under-delivery due to loss of insulin to an external leak. If insulin is not delivered properly, users may experience high blood glucose levels due to under-delivery of insulin. In the most severe cases, prolonged and persistent high blood glucose levels can lead to diabetic ketoacidosis (DKA), hyperglycemic hyperosmolar syndrome (HHS), or even death.

Jul 8, 2026Insulet Corporation
Medical Device
FDA DevicesClass II

ARTIS icono biplane. Model Number: 11327600.

Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.

Jul 8, 2026Siemens Medical Solutions USA, Inc
Medical Device
FDA DevicesClass II

Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjun...

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 tables.

Jul 8, 2026Baxter Healthcare Corporation
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Jul 8, 2026Medline Industries, LP
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026280 - FORD

Powertrain

Jul 8, 2026TC
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026281 - FORD

Powertrain

Jul 8, 2026TC
Food & Beverage
Germany BVLGeneral Alert

Salatkäse Kräuter

Krankheitserreger

Jul 8, 2026Hof Dannwisch, Dannwisch 1, 25358 Horst
Medical Device
FDA DevicesClass II

CRE Wireguided 6-8mm 240cm

Potential sterile breach of the pouches in which devices are packaged.

Jul 8, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE, Model Number: AR...

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality issues identified during a recent FDA manufacturing inspection of its drug manufacturing site.

Jul 8, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HA...

Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which will result in "exhalation obstructed " alarm, which may result in inadequate ventilation, oxygen desaturation. Advising: Prior to use, test lung action. If alarm occurs, expiratory valve set removal to overcome membrane adhesion or replacement

Jul 8, 2026Hamilton Medical AG
Medical Device
FDA DevicesClass II

CRE Pro Wireguided 6-8mm 240cm

Potential sterile breach of the pouches in which devices are packaged.

Jul 8, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass I

A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, sur...

Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

Jul 8, 2026Windstone Medical Packaging, Inc.
Medical Device
FDA DevicesClass II

CRE Pro Wireguided 8-10mm 240cm

Potential sterile breach of the pouches in which devices are packaged.

Jul 8, 2026Boston Scientific Corporation
Pharmaceutical
FDA DrugsClass II

BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl...

Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead distributed to customers outside of the intended distribution channel

Jul 8, 2026CareFusion 213, LLC
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