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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OE
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
XTANT Medical Holdings, Inc recalls nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D Adva
Hazard: Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
April 29, 2026Medical DevicesFDA
Davol, Inc. recalls Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.
Hazard: Potential for product to contain foreign matter, confirmed to be inspect fragments.
April 29, 2026Medical DevicesFDA
Magellan Diagnostics, Inc. recalls LeadCare Ultra Blood Lead Test Kit; Catalog Number: 70-8098; The LeadCare Ultra kit is provided with the following mat
Hazard: Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.
April 29, 2026Medical DevicesFDA
Magellan Diagnostics, Inc. recalls LeadCare¿ Plus Blood Lead Test Kit; Catalog Number: 82-0004; The LeadCare¿ Plus kit is provided with the following mat
Hazard: Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.
April 29, 2026Medical DevicesFDA
Magellan Diagnostics, Inc. recalls (1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, (4)LeadCare¿ II 9X Blood Lead Test Kit
Hazard: Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the LeadCare Test Systems. False positive lead results may cause delayed results and additional unnecessary testing.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ENSEMBLE GYNECO SCOPIE-LF DYNJ
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ARTERIOGRAM TRAY 00-402001T, 0
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADD A ENDOVASCULAR PACK-LF DYN
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes E P DRAPE PACK-LF DYNJ0373061J
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ARTHROSCOPY PACK DYNJ45173D
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EXTREMITY PACK DYNJ34846C
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes EYE PACK DYNJ35056A HEART
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ90939
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ANGIO KIT PACK DYNJ50783B
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes Medline Convenience Kits conta
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes FACE/RHINOPLASTY PACK DYNJ8034
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BARIATRIC DYNJ905153M, DYNJ9
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes MINOR ENT SINUS PACK-LF
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes BIOPSY PACK DYNJ38587A, DYNJ38
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes TAVR PACK DYNJ69246B ABDOMI
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes ADULT CATH PACK-LF DYNJ38395G
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes JUDKINS PACK DYNJ51126 AN
Hazard: Unapproved design changes to the products outside of the 510(k) clearance.
April 29, 2026Medical DevicesFDA
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM;
Hazard: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
April 29, 2026Medical DevicesFDA
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM;
Hazard: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
April 29, 2026Medical DevicesFDA
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10
Hazard: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
April 29, 2026Medical DevicesFDA
Angiodynamics, Inc. recalls AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM;
Hazard: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.