Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,401 - 2,425 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Olympus Inner Sheath, Long; Model No. WA22017T. Inner sheath for urological and gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1451-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR Software anomaly in the patient positioning system may result in positional discrepancy.	FDA Z-1430-2026	Medical Device	High	Mar 4, 2026 Recall: Feb 6, 2026	Details
Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1466-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Olympus Inner Sheath. Model No. A2642. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1456-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Resection Sheath. Model No. A22014A and A22014T. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1438-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION, Model Number: DYKM1361A; 2) TRUNK KIT 1EA, Model Number: DYKM2013; 3) TRUNK KIT 1EA, Model Number: DYKM2013A; 4) RN TRUNK KIT, Model Number: DYKM2699; 5) TRUNK KIT, Model Number: DYKTRUNK1 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1433-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details
Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MDSALINE7 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1431-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707 Knee and Humeral socket implants contain incorrect labeling.	FDA Z-1459-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 15, 2026	Details
Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A; Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.	FDA Z-1437-2026	Medical Device	High	Mar 4, 2026 Recall: Sep 13, 2024	Details
Olympus Resection Sheath, 26 Fr.; Model No. A22042A. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1443-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Campy CVA Medium 100/PK, R01272 Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.	FDA Z-1474-2026	Medical Device	High	Mar 4, 2026 Recall: Feb 5, 2026	Details
Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1441-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1453-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Olympus Resection Sheath. Model No. A2666T. for endoscopic diagnosis and treatment in urological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1457-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
PIE PAK Models: P2HC-A, P2HC-S, P2HC Lack of 510K clearance	FDA Z-1462-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 14, 2026	Details
Olympus Resection Inner Sheath for 26 Fr. Outer Sheath. Model No. A22040T. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1440-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1435-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details
Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1449-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR Software anomaly in the patient positioning system may result in positional discrepancy.	FDA Z-1429-2026	Medical Device	High	Mar 4, 2026 Recall: Feb 6, 2026	Details
Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1452-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036 Knee and Humeral socket implants contain incorrect labeling.	FDA Z-1460-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 15, 2026	Details
Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications. Complaints of the ceramic tip of the resection sheath breaking have been received.	FDA Z-1448-2026	Medical Device	High	Mar 4, 2026 Recall: Nov 11, 2025	Details
Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Medline DIALYSIS DRESSING CHANGE KIT SKU EBSI1107 EBSI1596 EBSI1781 EBSI1812 Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630 Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT SKU EBSI1470 Centurion VASCATH DRESSING CHANGE TRAY SKU DT22845 Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1467-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200 Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.	FDA Z-1463-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 8, 2026	Details
Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528 Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.	FDA Z-1434-2026	Medical Device	High	Mar 4, 2026 Recall: Jan 5, 2026	Details

Showing 2,401 - 2,425 of 3,321 product recalls

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