Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,351 - 2,375 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S in human citrated plasma by the immuno-turbidimetric method. Component: Not Applicable The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.	FDA Z-1491-2026	Medical Device	High	Mar 11, 2026 Recall: Feb 4, 2026	Details
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones. Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.	FDA Z-1477-2026	Medical Device	High	Mar 11, 2026 Recall: Nov 14, 2025	Details
Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.	FDA Z-1481-2026	Medical Device	High	Mar 11, 2026 Recall: Feb 2, 2026	Details
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.	FDA Z-1482-2026	Medical Device	High	Mar 11, 2026 Recall: Feb 2, 2026	Details
CS100 IABP. Software Version CS100 IABP Q.01. The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.	FDA Z-1486-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 23, 2026	Details
Atellica CH Urine Albumin (UAlb). Material Number: 11537225 Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may report values between 6.2 mg/dL and 40.0 mg/dL.	FDA Z-1484-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 20, 2026	Details
CS300 IABP. Software Version CS300 IABP C.01. The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.	FDA Z-1487-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 23, 2026	Details
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed,	FDA Z-1475-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 16, 2026	Details
cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, material number 08464502001 cobas pro SSU, material number 09205632001 Affected Assays: (Product Name/ Catalog Number/ Application Code/ Application Short Name) 1. Cystatin C Gen.2 08105596190 20510 CYSC2 2. Ferritin Gen.4 08057648190 20571 FER4X 3. Lipoprotein (a) Gen.2 08106126190 20861 LPA2X 4. Lipoprotein (a) molarity 08106126160 20864 LPA2-X 5. Vancomycin Gen.3 08058849190 21211 VANC3O 6. Kappa Free Light Chains Partner Channel 08896640190 21421 KFLCX 7. Lambda Free Light Chains Partner Channel Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an automated analyzer, intended for running qualitative, semi-quantitative and quantitative clinical chemistry and immunochemistry assays, as well as ion-selective measurements. When an erroneous calibration is active, the instrument fails to calculate new values and instead repeats the last successfully calculated result from any Spline-type assay for all subsequent measurements, leading to identical and erroneous patient and QC results. The defect could lead to patients receiving erroneous lab results, which could result in a remote risk of serious adverse health consequences. The following assays use spline type calibration and are affected by this issue: Cystatin C Gen.2, Ferritin Gen.4, Lipoprotein (a) Gen. 2, Lipoprotein (a) molarity, Vancomycin Gen.3, Kappa Free Light Chains Partner Channel, Lambda Free Light Chains Partner Channel, and fCAL turbo Partner Channel.	FDA Z-1476-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 20, 2026	Details
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038 A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.	FDA Z-1490-2026	Medical Device	High	Mar 11, 2026 Recall: Mar 14, 2025	Details
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A There is the potential for the length of the trocar shaft to be too long.	FDA Z-1485-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 15, 2026	Details
EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5 Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length lenses, so there is the potential for excessive vault, which may cause: Significant reduction of irido-corneal angles, Significant shallowing of anterior chamber, Patient discomfort, Elevated IOP/Angle closure, Unreactive pupil, Lens exchange/removal.	FDA Z-1480-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 21, 2026	Details
Impella RP. Product Code: 0046-0011. Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.	FDA Z-1471-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 27, 2026	Details
Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.	FDA Z-1483-2026	Medical Device	High	Mar 11, 2026 Recall: Feb 2, 2026	Details
Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones. Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.	FDA Z-1479-2026	Medical Device	High	Mar 11, 2026 Recall: Nov 14, 2025	Details
Impella RP with SmartAssist. Product Code: 0046-0035. Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.	FDA Z-1469-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 27, 2026	Details
Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids. Potential for rubber fragment detachment during use.	FDA Z-1489-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 29, 2026	Details
Impella RP Flex with SmartAssist. Product Code: 1000323. Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.	FDA Z-1470-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 27, 2026	Details
Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids. Potential for rubber fragment detachment during use.	FDA Z-1488-2026	Medical Device	High	Mar 11, 2026 Recall: Jan 29, 2026	Details
Premium Food Bubble Gum, packed in 2.5 oz clear flexible plastic packaging, all lots and codes. Sold in unit case of 30 LB. Contains undeclared colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).	FDA H-0539-2026	Food	High	Mar 11, 2026 Recall: Jan 16, 2026	Details
Lobster & Crab Ravioli. Keep Frozen. Contains: Wheat, Eggs, Milk, Crustaceans-Shellfish. Product is intended to be further cooked. Weight: 1-10 pound (4.5g). Use within 6 months. 801-541-9292-www.FunarosPerfectPasta.com. 1391 So. 300 West Slc, Ut 84115. Undeclared shrimp, crab, lobster, pollock (fish), whiting (fish), and soy.	FDA H-0620-2026	Food	High	Mar 11, 2026 Recall: Feb 8, 2026	Details
Premium Food Jordan Almonds, packed in 2.0 oz and 3.5 oz clear flexible plastic packaging. Contains undeclared allergen (wheat) and colors (FD&C Blue 1 Lake and FD&C Blue 2 Lake).	FDA H-0538-2026	Food	High	Mar 11, 2026 Recall: Jan 16, 2026	Details
Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakout Product may contain undeclared peanuts.	FDA H-0574-2026	Food	High	Mar 11, 2026 Recall: Jan 30, 2026	Details
VERGANI 1944 MILANO 'PANDORO CLASSICO' Gluten Free, 600g NET WT. 1 LBS. 5.2 OZ., packaged in paper cartons, 6 units per case. Lot 217666, UPC 8002114019833 Potential contamination with foreign material (Teflon fragments) from flaking cooking molds.	FDA H-0540-2026	Food	High	Mar 11, 2026 Recall: Feb 10, 2026	Details
Junebar Peanut Chocolate Chip All Natural Snack Bar; INGREDIENTS: ORGANIC PEANUT BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN SHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), PEANUTS, OAT FLOUR, VANILLA EXTRACT (VANILLA BEAN EXTRATIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS PEANUTS, TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUIPMENT ALSO HANDLING PEANUT, SESAME, PRODUCED IN A FACILITY THAT ALSO PROCESSES GLUTEN PRODUCTS. KEEP REFRIGERATED.; UPC 8 600 Products contain undeclared milk and soy.	FDA H-0542-2026	Food	High	Mar 11, 2026 Recall: Feb 11, 2026	Details

Showing 2,351 - 2,375 of 3,321 product recalls

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