Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Showing 24 of 74,116 results
Pharmaceutical
FDA Drugs
FDA DrugsfentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.
Wells Pharma of Houston LLC
FDA DrugsClass II
fentaNYL Citrate Injectable Solution in 0.9% Sodium Chloride, 1000 mcg/50mL (20 mcg per mL), well pharma of Houston, NDC 73702-203-65.
cGMP deviations.
May 6, 2026Wells Pharma of Houston LLC
Medical DeviceFDA Devices
FDA DevicesDepuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.
DEPUY (IRELAND)
FDA DevicesClass II
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
May 6, 2026DEPUY (IRELAND)
PharmaceuticalFDA Drugs
FDA DrugsKetamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
Wells Pharma of Houston LLC
FDA DrugsClass II
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
cGMP deviations.
May 6, 2026Wells Pharma of Houston LLC
PharmaceuticalFDA Drugs
FDA DrugsfentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
Wells Pharma of Houston LLC
FDA DrugsClass II
fentaNYL Citrate Injectable Solution, NARCOTIC, Cii, 1000 mcg/100 mL (10 mcg per mL), 100 mL bag, Wells Pharma in Houston, NDC 73702-202-02.
cGMP deviations.
May 6, 2026Wells Pharma of Houston LLC
Medical DeviceFDA Devices
FDA DevicesStraumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
Straumann USA LLC
FDA DevicesClass II
Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
Includes an incorrect screw seat interface.
May 6, 2026Straumann USA LLC
Medical DeviceFDA Devices
FDA DevicesWHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
WHILL, INC.
FDA DevicesClass I
WHILL Model C2, with software versions before HMI: 2.22 / MC: 1.13; device is an indoor/outdoor battery-operated 2-wheel drive (rear-wheel drive) powered wheelchair.
Cyber vulnerability of BLE communication was found by CISA VDP program.
May 6, 2026WHILL, INC.
Medical DeviceFDA Devices
FDA DevicesPhilips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.
Philips North America
FDA DevicesClass II
Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF): 782144. 3. Model Number (REF): 782163.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
May 6, 2026Philips North America
Medical DeviceFDA Devices
FDA DevicesMedline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U
Medline Industries, LP
FDA DevicesClass II
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: ANGIO PACK-LF, Medline Kit Number/SKU DYNJ0774765U
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
May 6, 2026Medline Industries, LP
Medical DeviceFDA Devices
FDA DevicesVACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS
Milestone S.R.L.
FDA DevicesClass II
VACUUM BAG SU LARGE, Non-sterile specimen container, Model/Catalog Number: 68409SS
There is a possibility of reagent leakage from the specimen container.
May 6, 2026Milestone S.R.L.
Medical DeviceFDA Devices
FDA DevicesMedline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. FOLEY CARE KIT, Medline Kit SKU UROT1044; 2. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770; 3. IV START KIT, Medline Kit SKU DYNDV2520; 4. ARTERIAL LINE BUNDLE, Medline Kit SKU ART255; 5. ON/OFF TRAY, Medline Kit SKU DYNDC2969; 6. IV START KIT, Medline Kit SKU DYNDV2520; 7. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770; 8. (Centurion) ARTERIAL LINE BUNDLE, Medline Kit SKU ART255; 9. ON/OFF TRAY, Medline Kit SKU DYNDC2969; 10. CVAD DRESSING CHANGE KIT, Medline Kit SKU EBSI1364A.
Medline Industries, LP
FDA DevicesClass II
Medline and Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. FOLEY CARE KIT, Medline Kit SKU UROT1044; 2. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770; 3. IV START KIT, Medline Kit SKU DYNDV2520; 4. ARTERIAL LINE BUNDLE, Medline Kit SKU ART255; 5. ON/OFF TRAY, Medline Kit SKU DYNDC2969; 6. IV START KIT, Medline Kit SKU DYNDV2520; 7. IV START KIT WITH EXTENSION TUBING, Medline Kit SKU IV8770; 8. (Centurion) ARTERIAL LINE BUNDLE, Medline Kit SKU ART255; 9. ON/OFF TRAY, Medline Kit SKU DYNDC2969; 10. CVAD DRESSING CHANGE KIT, Medline Kit SKU EBSI1364A.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
May 6, 2026Medline Industries, LP
PharmaceuticalFDA Drugs
FDA DrugsLidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
Water-Jel Technologies, LLC
FDA DrugsClass III
Lidocaine Wound Gel (Benzalkonium Chloride, 0.13% and Lidocaine Hydrochloride, 2%), NET WT 0.5 OZ (14 g), Distributed by: CVS PHarmacy, INc., One CVS Drive, Woonsocket, RI 02895. NDC 59898-950
Failed PH Specifications
May 6, 2026Water-Jel Technologies, LLC
PharmaceuticalFDA Drugs
FDA DrugsGenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, Inc., Fort Worth, Texas 76134, USA, NDC: 0065-8064-01.
Alcon Research LLC
FDA DrugsClass II
GenTeal Tears, Lubricant Eye Gel, Sterile, 10g (0.34 Fl oz), Distributed by: Alcon Laboratories, Inc., Fort Worth, Texas 76134, USA, NDC: 0065-8064-01.
Lack of Assurance of Sterility: Due to FDA inspection observations that it believes may impact product quality.
May 6, 2026Alcon Research LLC
Medical DeviceFDA Devices
FDA DevicesMedline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: CERVICAL PACK, Medline Kit Number/SKU DYNJ37902F
Medline Industries, LP
FDA DevicesClass II
Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: CERVICAL PACK, Medline Kit Number/SKU DYNJ37902F
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
May 6, 2026Medline Industries, LP
Safety Alert
Health Canada
Health CanadaHealth Canada warns that Gedsffati Plug-in Combined Smoke and Carbon Monoxide Alarm previously available on Amazon.ca may fail to operate
Consumer product safety
Health CanadaGeneral Alert
Health Canada warns that Gedsffati Plug-in Combined Smoke and Carbon Monoxide Alarm previously available on Amazon.ca may fail to operate
Unauthorized products
May 6, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaGermina brand "Brocoli Calabrese" seeds recalled due to pathogenic E. coli
CFIA
Health CanadaClass 1
Germina brand "Brocoli Calabrese" seeds recalled due to pathogenic E. coli
E. Coli - other pathogenic
May 6, 2026CFIA
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026086 - GENERAL MOTORS
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026086 - GENERAL MOTORS
Other
May 6, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026152 - NOVA BUS
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026152 - NOVA BUS
Structure
May 6, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026166 - GENERAL MOTORS
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026166 - GENERAL MOTORS
Visual System
May 6, 2026TC
Safety AlertHealth Canada
Health CanadaJia Fu Li brand Wasabi Green Peas recalled due to improperly declared soy
CFIA
Health CanadaClass 2
Jia Fu Li brand Wasabi Green Peas recalled due to improperly declared soy
Soy
May 6, 2026CFIA
Safety AlertHealth Canada
Health CanadaM Zn-Air Battery Pak
Medical devices
Health CanadaType II
M Zn-Air Battery Pak
Performance
May 6, 2026Medical devices
Safety AlertHealth Canada
Health CanadaSperti™ Vitamin D Lamp
Medical devices
Health CanadaType II
Sperti™ Vitamin D Lamp
Unauthorised device
May 6, 2026Medical devices
Safety AlertHealth Canada
Health CanadaBard SILASTIC® Foley Catheter
Medical devices
Health CanadaType II
Bard SILASTIC® Foley Catheter
Performance
May 6, 2026Medical devices
Safety AlertHealth Canada
Health CanadaMOSAIQ
Medical devices
Health CanadaType II
MOSAIQ
Performance
May 6, 2026Medical devices
Safety AlertHealth Canada
Health CanadaAzurion and Allura Xper Systems
Medical devices
Health CanadaType II
Azurion and Allura Xper Systems
Performance
May 6, 2026Medical devices