Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Showing 24 of 74,115 results
Medical Device
FDA Devices
FDA DevicesMEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use
BD SWITZERLAND SARL
FDA DevicesClass II
MEDLINE 111 GRAVITY SET W/3 Needle Free Y-Sites REF DYNDTN0555 Catalog Number: SAM2461 UDI code: N/A Engineering Sample/Not for Human Use
Due to engineering sample labeled "Not for Human Use" being inadvertently shipped it the U.S. market.
Jul 8, 2026BD SWITZERLAND SARL
Medical DeviceFDA Devices
FDA DevicesReprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.
Medline Industries, LP
FDA DevicesClass I
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.
Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection. If particulate were to dislodge during use and contact circulating blood or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Jul 8, 2026Medline Industries, LP
Medical DeviceFDA Devices
FDA DevicesCyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Accuray Incorporated
FDA DevicesClass II
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
Jul 8, 2026Accuray Incorporated
Medical DeviceFDA Devices
FDA DevicesMedline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1699A
Medline Industries, LP
FDA DevicesClass II
Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY, Model Number: PAIN1699A
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 DeviceFDA Devices
FDA DevicesDepuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 10mm B; Part Number: 151730410. 2. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 12mm B; Part Number: 151730412. 3. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 14mm B; Part Number: 151730414. 4. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 16mm B; Part Number: 151730416. 5. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 18mm B; Part Number: 151730418. 6. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 20mm B; Part Number: 151730420. 7. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 22mm B; Part Number: 151730422. 8. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 24mm B; Part Number: 151730424. 9. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 26mm B; Part Number: 151730426. 10. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 8mm B; Part Number: 151730408. 11. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 10mm C; Part Number: 151730510. 12. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 12mm C; Part Number: 151730512. 13. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 14mm C; Part Number: 151730514. 14. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 16mm C; Part Number: 151730516. 15. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 18mm C; Part Number: 151730518. 16. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 20mm C; Part Number: 151730520. 17. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 22mm C; Part Number: 151730522. 18. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 24mm C; Part Number: 151730524. 19. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 26mm C; Part Number: 151730526. 20. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 8mm C; Part Number: 151730508. 21. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 10mm E; Part Number: 151730710. 22. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 12mm E; Part Number: 151730712. 23. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 14mm E; Part Number: 151730714. 24. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 16mm E; Part Number: 151730716. 25. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 18mm E; Part Number: 151730718. 26. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 20mm E; Part Number: 151730720. 27. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 22mm E; Part Number: 151730722. 28. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 24mm E; Part Number: 151730724. 29. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 26mm E; Part Number: 151730726. 30. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 8mm E; Part Number: 151730708. 31. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 10mm W; Part Number: 151730810. 32. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 12mm W; Part Number: 151730812. 33. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 14mm W; Part Number: 151730814. 34. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 16mm W; Part Number: 151730816. 35. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 18mm W; Part Number: 151730818. 36. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 20mm W; Part Number: 151730820. 37. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 22mm W; Part Number: 151730822. 38. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 8mm F; Part Number: 151730808. 39. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 24mm W; Part Number: 151730824. 40. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 26mm W; Part Number: 151730826.
DEPUY (IRELAND)
FDA DevicesClass II
Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 10mm B; Part Number: 151730410. 2. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 12mm B; Part Number: 151730412. 3. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 14mm B; Part Number: 151730414. 4. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 16mm B; Part Number: 151730416. 5. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 18mm B; Part Number: 151730418. 6. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 20mm B; Part Number: 151730420. 7. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 22mm B; Part Number: 151730422. 8. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 24mm B; Part Number: 151730424. 9. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 26mm B; Part Number: 151730426. 10. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 4 8mm B; Part Number: 151730408. 11. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 10mm C; Part Number: 151730510. 12. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 12mm C; Part Number: 151730512. 13. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 14mm C; Part Number: 151730514. 14. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 16mm C; Part Number: 151730516. 15. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 18mm C; Part Number: 151730518. 16. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 20mm C; Part Number: 151730520. 17. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 22mm C; Part Number: 151730522. 18. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 24mm C; Part Number: 151730524. 19. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 26mm C; Part Number: 151730526. 20. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 5 8mm C; Part Number: 151730508. 21. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 10mm E; Part Number: 151730710. 22. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 12mm E; Part Number: 151730712. 23. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 14mm E; Part Number: 151730714. 24. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 16mm E; Part Number: 151730716. 25. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 18mm E; Part Number: 151730718. 26. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 20mm E; Part Number: 151730720. 27. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 22mm E; Part Number: 151730722. 28. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 24mm E; Part Number: 151730724. 29. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 26mm E; Part Number: 151730726. 30. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 7 8mm E; Part Number: 151730708. 31. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 10mm W; Part Number: 151730810. 32. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 12mm W; Part Number: 151730812. 33. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 14mm W; Part Number: 151730814. 34. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 16mm W; Part Number: 151730816. 35. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 18mm W; Part Number: 151730818. 36. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 20mm W; Part Number: 151730820. 37. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 22mm W; Part Number: 151730822. 38. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 8mm F; Part Number: 151730808. 39. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 24mm W; Part Number: 151730824. 40. ATTUNE KNEE SYSTEM REVISION HINGE INSERT 8 26mm W; Part Number: 151730826.
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Jul 8, 2026DEPUY (IRELAND)
Medical DeviceFDA Devices
FDA DevicesA M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
Windstone Medical Packaging, Inc.
FDA DevicesClass I
A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
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.
Safety Alert
Health Canada
Health CanadaTwo lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
Communications and Public Affairs Branch
Health CanadaType I
Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
Product quality
Jul 8, 2026Communications and Public Affairs Branch
Medical DeviceFDA Devices
FDA DevicesCRE Wireguided 6-8mm 240cm
Boston Scientific Corporation
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 DeviceFDA Devices
FDA DevicesCRE Wireguided 12-15mm 240cm
Boston Scientific Corporation
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 DeviceFDA Devices
FDA DevicesCRE Wireguided 15-18mm 240cm
Boston Scientific Corporation
FDA DevicesClass II
CRE Wireguided 15-18mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
Jul 8, 2026Boston Scientific Corporation
Medical DeviceFDA Devices
FDA DevicesMedline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590
Medline Industries, LP
FDA DevicesClass II
Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590
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
RappelConso
RappelConsorenault - austral voiture particulière
renault
RappelConsoGeneral Alert
renault - austral voiture particulière
l'unité de commande abs-esp peut avoir été mal programmée par le fournisseur, empêchant la communication des défaillances détectées au tableau de bord du véhicule. en conséquence, en cas de défaillance du système de commande de freinage, il se peut que le conducteur ne reçoive pas d'avertissement indiquant que les fonctions suivantes ne sont pas disponibles: l’assistance au freinage d’urgence, le système de freinage antiblocage (abs), le programme électronique de stabilité (esp), le freinage d’urgence automatique (aeb), l’amplificateur de frein hydraulique (hbb) et la compensation du freinage hydraulique (hbc), ce qui augmente le risque d’accident.
Jul 8, 2026renault
Food & BeverageRappelConso
RappelConsopas de marque. - herbes épices bbq
pas de marque.
RappelConsovolontaire (san...
pas de marque. - herbes épices bbq
résidus de pesticides.
Jul 8, 2026pas de marque.
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026309 - AIRSTREAM
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026309 - AIRSTREAM
Electrical
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026283 - FORD
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026283 - FORD
Powertrain
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026306 - FOREST RIVER
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026306 - FOREST RIVER
Electrical
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026282 - FORD
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026282 - FORD
Other
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026303 - BRAUNABILITY
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026303 - BRAUNABILITY
Airbag
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026296 - FOREST RIVER
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026296 - FOREST RIVER
Label
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026307 - GENERAL MOTORS
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026307 - GENERAL MOTORS
Steering
Jul 8, 2026TC
Safety AlertHealth Canada
Health CanadaTAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns
Marketed health products
Health CanadaGeneral Alert
TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns
New safety information - Product safety
Jul 7, 2026Marketed health products
Safety AlertHealth Canada
Health CanadaGummy Gainz brand Protein Candy recalled due to improperly declared milk
CFIA
Health CanadaClass 1
Gummy Gainz brand Protein Candy recalled due to improperly declared milk
Milk
Jul 7, 2026CFIA
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026305 - INDIAN
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026305 - INDIAN
Label
Jul 7, 2026TC
Safety AlertHealth Canada
Health CanadaSunluway Oven Bottom Panel Replacement recalled due to burn hazard
Consumer product safety
Health CanadaGeneral Alert
Sunluway Oven Bottom Panel Replacement recalled due to burn hazard
Burn hazard
Jul 7, 2026Consumer product safety