Every recall we track for Riverpoint Medical, LLC — 44 in all — plus the complaints and injury reports the public filed about them.
Riverpoint Medical recalls Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black/Black/White) due to risk of suture breaks from insertion failures in hard bone conditions. Affected units may cause damage to the suture construct during surgery.
Riverpoint Medical recalls Covidien CV-9590 Velosorb sutures with potential weak strength that could cause breaks during surgery or wound separation. Affected units have specific lot numbers and sizes.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture due to non-sterile condition, which could cause surgical site infections. Affected products include specific lot numbers and sizes.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could increase surgical site infections. Affected units have UDI 20884521150918.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could increase surgical site infections and break strength retention risks. Affected units include specific product numbers and lot numbers.
Riverpoint Medical recalls Velosorb 4/0 absorbable suture due to non-sterile condition, which could cause surgical site infections. Affected units have UDI 20884521151731.
Riverpoint Medical recalls Velosorb 4/0 undyed 18" PC-10 sutures due to non-sterile condition, which could increase surgical site infections. Affected units have Product Number SV835G and were sold starting in 2006.
Riverpoint Medical recalls Velosorb 4/0 undyed 30" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SV426 and UDI 20884521151731.
Riverpoint Medical recalls non-sterile Velosorb 2/0 suture to prevent surgical infections. Affected items have specific UDI and lot numbers.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture due to non-sterile condition, which could increase surgical site infections and break strength retention risks. Affected units have specific product numbers and lot numbers.
Riverpoint Medical recalls non-sterile Velosorb 3/0 absorbable suture to prevent surgical site infections. The suture may compromise sterile field during procedures.
Riverpoint Medical recalls non-sterile Velosorb 4/0 suture (product SV9911G) due to infection risks. Affected units sold in 2023; stop using if used in surgery.
Riverpoint Medical recalls Velosorb 4/0 undyed suture due to non-sterile condition, which could cause surgical site infections. Affected units have Product Number SV496 and Lot Number 20060116FX.
Riverpoint Medical recalls non-sterile Velosorb 4/0 suture (product # SVP2251) due to infection risk. Affected units sold with specific lot number. Stop using immediately to prevent surgical site infections.
Riverpoint Medical recalls Velosorb 4/0 undyed 30" suture (product SV2294) due to non-sterile condition, which may cause surgical site infections. Affected units sold with UDI 20884521151403.
Riverpoint Medical recalls Velosorb 4/0 undyed 18" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have product number SV496G and lot number 20052721FX.
Riverpoint Medical recalls non-sterile Velosorb 5/0 absorbable suture due to infection risk. Affected units have product number CV1213 and lot 20052817X. Stop using if used in surgery.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have UDI 20884521177410.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture due to non-sterile condition, which could increase surgical site infection risk. Learn if you have the affected product and what to do.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture (Product SV2239) due to non-sterile condition, which may cause surgical site infections. Affected units were sold with specific lot numbers.
Riverpoint Medical recalls Velosorb 3/0 absorbable sutures due to non-sterile condition, which may increase surgical site infections. Affected products include specific lot numbers and product codes.
Riverpoint Medical recalls non-sterile Velosorb 3/0 absorbable suture (Product CV416G) due to infection risk. This suture may cause surgical site infections if not sterile.
Riverpoint Medical recalls non-sterile Velosorb surgical suture that could cause infections during procedures. Affected units have product number CV947 and were sold in 2023. Contact for replacement.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which can cause surgical site infections. Affected units have UDI 20884521151021. Stop using immediately to prevent infection risks.
Riverpoint Medical recalls Velos: non-sterile surgical suture that could cause infections during procedures. Affected units have UDI 20884521149707. Stop using immediately to avoid infection risks.
Riverpoint Medical recalls non-sterile Velosorb 6/0 suture due to infection risk. Stop using if you have this product to avoid surgical site infections.
Riverpoint Medical recalls non-sterile Velosorb 2/0 absorbable suture (Product CV417G) due to infection risk in surgeries. Affected units may cause surgical site infections if used without proper sterility.
Riverpoint Medical recalls Velosorb 4/0 undyed 30" absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SVP2294 and Lot Number 20052017FX.
Riverpoint Medical recalls Velosorb 6/0 absorbable sutures due to non-sterile condition, which may cause surgical site infections. Affected products include specific lot numbers and product codes.
Riverpoint Medical recalls Velosorb 3/0 undyed suture due to non-sterile condition, which may cause surgical site infections. Affected units have Product Number SV935 and UDI 20884521151755.
Riverpoint Medical recalls non-sterile Velosorb 6/0 VL 18" P-10 sutures due to infection risk. Affected units have Product Number SV32 and UDI 20884521153117. Stop using if used in surgery.
Riverpoint Medical recalls Velos: non-sterile surgical suture that could cause infections during procedures. Affected units have specific product numbers and lot dates.
Riverpoint Medical recalls Velosorb 4/0 absorbable sutures due to non-sterile condition, which may cause surgical site infections. Affected units have specific lot numbers and UDI codes.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture due to non-sterile condition, which could increase surgical site infections. Affected units have specific UDI and lot numbers.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have specific UDI and lot numbers.
Riverpoint Medical recalls non-sterile Velosorb 3/0 absorbable suture (product CV3110) due to infection risk. Use may compromise sterile field and cause surgical site infections.
Riverpoint Medical recalls Velosorb 3/0 absorbable suture due to non-sterile condition, which could lead to surgical site infections. Affected units have UDI 1088452:1149595.
Riverpoint Medical recalls Velosorb Fast Braided Absorbable Suture due to non-sterile condition, which could cause surgical site infections. Affected units have UDI: 20884521152288.
Riverpoint Medical recalls non-sterile Velosorb surgical suture that could cause infections during procedures. Affected units have specific UDI and lot numbers. Consumers should contact the manufacturer for details.
Riverpoint Medical recalls non-sterile Velosorb 4/0 suture to prevent surgical site infections. The recall affects specific product numbers sold in 2023. Consumers should check labels for product number CV3100.
Riverpoint Medical recalls Velosorb 4/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have UDI 20884521151731.
Riverpoint Medical recalls Velosorb 5/0 absorbable suture due to non-sterile condition, which may cause surgical site infections. Affected units have product number CV2293 and lot 20060118X.
Riverpoint Medical recalls 18G Brachy Grid (RPG-18) due to potential sterile packaging compromise. Affected units have specific lot numbers and UDI. Consumers should contact for details.
Riverpoint Medical recalls 18G Brachy Grid (RPG-18) due to lack of EU approval. This device is used in brachytherapy procedures but is not approved for sale in the European Union.
