Recalls in Florida (page 17)
4115 recalls.
- CRE Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - Medtronic Harmony Delivery Catheter System recall (Medtronic Heart Valves Division)
Medical deviceClass IReported July 8, 2026 · Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system... - GC Agar Base recall (Remel, Inc)
Medical deviceClass IIReported July 8, 2026 · Reduced or no recovery of some strains of Neisseria gonorrhoeae. - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH recall (Medline Industries, LP)
Medical deviceClass IReported July 8, 2026 · Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on... - Omnipod recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.... recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA P.CIRCUIT 5KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) ARTERIAL LINE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) SUTURE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) SUTURING SET recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) IMAGING BIOPSY TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) STD recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) DYNJ0621189X recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) MULTIMED recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) BLOCK TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · 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... - Winco Fireworks International Recalls Roman Candles 8 Shot Fireworks Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 3, 2026 · The recalled fireworks can malfunction, and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. - Winco Fireworks International Recalls Unity 7 Shot 200 Gram Aerial Cake Fireworks Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 3, 2026 · The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards. - Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
Consumer productReported July 3, 2026 · Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that... - Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store
Consumer productReported July 3, 2026 · The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin... - Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fire Hazard
Consumer productReported July 3, 2026 · The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard. - Target Recalls Gigglescape™ Under the Sea Popping Toy Due to Choking Hazard
Consumer productReported July 3, 2026 · The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard. - AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions; Sold on Amazon by Pretty-Life
Consumer productReported July 3, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support... - Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported July 3, 2026 · The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards. - Projecting LED Finger Light Toys Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by POPOOO
Consumer productReported July 3, 2026 · The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by... - Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported July 3, 2026 · The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging... - Topyond Pool Drain Ports with Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold by Jialyduu
Consumer productReported July 3, 2026 · The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly... - Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for Infant Sleep Products
Consumer productReported July 3, 2026 · The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed... - 25# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/NS recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 8/9.5oz Tub Nut - Sunflower Seed recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz No Salt Sunflower Seeds recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz Sunflower Seeds Salted recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 2.0 oz Dirty Sour Cream and Onion Potato Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.0 oz Dirty Maui Onion Chip recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - Dried Herring Fish 7 oz. recall (Prime Food Processing LLC.)
FoodClass IReported July 1, 2026 · Improperly eviscerated which may result in Clostridium botulinum contamination - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. KIT... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).