Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 14,401–14,450 of 15,379
- Class II
Medical Device Recall · December 20, 2023
Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class I
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 18Fr., 48in Long, REF EN0046180BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube and PreVent¿ Anti-Reflux Filter and Lopez Valve¿ with ENFit, 12Fr., 48in Long, REF EN0056120BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube with ENFit, 18Fr., 48in Long, REF EN0042180BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 14Fr., 48in Long, REF EN0046140BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube and PreVent¿ Filter and Lopez Valve¿ with ENFit, 14Fr., 48in Long, REF EN0056140BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Food Recall · December 20, 2023
LuLu Chinese Express, Sweet and Sour Shrimp w/ Fried Rice, Net Wt. 16 oz (1 lb), UPC 2393329006, packaged in plastic container.Soy is missing from the "Contains" statement.
- Class I
Food Recall · December 20, 2023
Shennongyuan Dried Longan packaged in a silver metal box bulk 18kgsProduct contains undeclared sulfites.
- Class I
Food Recall · December 20, 2023
Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per caseThe firm initiated a recall of SoyBean Sprouts because product tested positive for Listeria monocytogenes.
- Class II
Medical Device Recall · December 20, 2023
Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 10Fr., 36in Long, REF EN0046100BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- Class II
Medical Device Recall · December 20, 2023
Barco MDSC-8527 NXF, Part Number K9352421Barco became aware of a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. The functionality of the built-in MNA decoder is blocked.
- Class II
Medical Device Recall · December 20, 2023
Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide intravenous infusion of parenteral fluids, blood and blood products to a patient under the direction or supervision of physician or oWhen utlizing the patient query feature on the Zyno Medical Z-800WF pumps with software version 5.2.05, the alarm volume may inadvertently revert from a higher volume setting to a low one, causing potential delays in therapy and in extreme cases, associated risk of organ failure or death
- Class I
Food Recall · December 19, 2023
Ministry of Snacks Sweet and Savory Collection #8700Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed in gift baskets.
- Class II
Medical Device Recall · December 19, 2023
REV 2 Flowcell Capsule Spare, Part Number: C04154Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.
- Class II
Food Recall · December 19, 2023
Cheddar Kettle Corn, Net Wt 10 Oz (283 g), Ingredients: Locally-Farmed Corn, Corn Oil, Sugar, Salt, 100% Cheddar PowderCheddar Popcorn label does not declare milk or sub-ingredients, Maltodextrin, Sunflower oil, Yellow #5, Yellow #6, and Lactic Acid.
- Class II
Medical Device Recall · December 19, 2023
Smiths Medical Medfusion Model 3500 Syringe pumps, Item Numbers: a) 3500 b) 3500-0600-00 c) 3500-0600-01 d) 3500-0600-249 e) 3500-0600-50 f) 3500-0600-51 g) 3500-0600-82 h) 3500-306 i) 3500Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
- Class II
Medical Device Recall · December 19, 2023
Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S Acu-Loc VDU Plate Standard, Left; 70-0046 Acu-Loc VDU Plate StandarDistribution without Pre-Market Clearance
- Class II
Medical Device Recall · December 19, 2023
Smiths Medical Model 3010 Syringe pumps: a. Protege Model 3010, b. Medfusion Model 3010A, c. Protege UK Model 3010EMedfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
- Class II
Medical Device Recall · December 19, 2023
Model A710 Intellis Clinician Programmer Application, version 2.0.97Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.
- Class II
Medical Device Recall · December 19, 2023
Smiths Medical Medfusion Guide Barrel Clamp, Item number G6000716Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
- Class II
Medical Device Recall · December 19, 2023
Accessory Sets Syringes: 6ml syringe with a female luer with 15cm sealed SCD tubing, REF: RF-T15, and 60ml syringe on a female luer with 15cm sealed SCD tubing, REF: 15-RF60-TAccessory sets contain a syringes not yet qualified for the accessory's intended purpose; due to design changes to the syringe barrels and a polypropylene resin change that resulted in loss of gamma compatibility, for accessory set syringes that were gamma sterilized, which resulted in yellowed syringes.
- Class II
Medical Device Recall · December 19, 2023
iQ Waste Well Adapter, Part Number: 700-3393Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.
- Class II
Medical Device Recall · December 19, 2023
EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM, Outer Box UPN M00509500 or M00509510.Affected batches of the kit contain Stoma Measuring Devices sized to measure for an 18/24F replacement button, but are labeled as being for a 28F. Use of defective product may lead to undersizing the button, which may cause embedding with erosion into the gastric wall, tissue necrosis, infection, sepsis, and associate sequelae.
- Class I
Medical Device Recall · December 19, 2023
smiths medical Medfusion Model 3500 Syringe pumpMedfusion syringe pumps, with software versions before v6.0.0, may have the following issues:1. Delivery During Motor Not Running High Priority Alarm, 2. Infusion Restarted with Incorrect Parameters, 3. Screen Lock, 4. Interruption of Bolus or Loading Dose Delivery, 5. Pump Displays Incorrect Bolus/Loading Dose, 6. Loading/Bolus Dose Below the Minimum Recommended Rate, 7. Motor Rate Error, 8. Incorrect Recall Last Settings, 9. Corrupt Configuration, 10. Auto Lock, 11. Toolbox Configuration Loading Dose Time Values. Smiths Medical corrected all issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent Medfusion software (v6.0.0) installed on your pumps.
- Class II
Medical Device Recall · December 19, 2023
Smiths Medical Medfusion Model 4000 Syringe pump, Item Numbers: a) 4000-0101-249, b) 4000-0101-50, c) 4000-0101-51, d) 4000-0105-249, e) 4000-0105-50, f) 4000-0105-51, g) 4000-0105-78,Medfusion Model 4000, 3500, and 3010 pumps manufactured or serviced with Barrel Clamp Guide (Part Number G6000716), Lot Numbers P0407365, P0486670, and P0561740 may contain a molding defect that could potentially lead to slippage of the spring within the barrel clamp assembly. If this occurs, it could result in the inability of the pump to recognize a syringe or the pump may misidentify the size of the syringe loaded.
- Class II
Medical Device Recall · December 19, 2023
Beckman Coulter DxU 850m/840m Microscopy Analyzers, Part Numbers: C49513, C76947Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.
- Class I
Medical Device Recall · December 19, 2023
smiths medical Medfusion Model 4000 syringe pumpMedfusion Model 4000 syringe infusion pumps, with the following software versions, may have the following issues: 1. Delivery During Motor Not Running High Priority Alarm (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 2. Re-administered Loading Dose (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 3. Incorrect Critical Data Failure Alarm, 4. Interruption of Bolus or Loading Dose Delivery (v1.0.0, v1.1.0, v1.1.1, v1.1.2), 5. Incorrect Total Bolus/Loading Dose Displayed (v1.1.0, v1.1.1, v1.1.2), 6. Volume Limit Before Bolus/Loading Dose Complete (v1.1.2), 7. Drug Library Lower Limit Displayed Incorrectly (v1.6.0, v1.6.1), 8. Depleted Battery Alarm (All versions previous to v1.6.5), 9. Loss of Wireless Connectivity (v1.5.0, v1.5.1, v1.6.0, v1.6.1, v1.6.4), 10. PharmGuard Server Password (v2.3, v2.4, v2.5). Smiths Medical corrected all issues included in this notification in previous software updates and the corrections were carried forward into all subsequent software releases. Please ensure you have the most recent Medfusion software installed on your pumps.
- Class II
Medical Device Recall · December 19, 2023
iQ200 Series Urine Microscopy Analyzers, Part Numbers: a) 700-3320, b) 700-3370, c) 700-3345, d) 700-3347, e) C10683, f) 700-3375, g) 700-3325, h) C10684Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.
- Class III
Food Recall · December 18, 2023
Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
- Class III
Food Recall · December 18, 2023
Shiloh Farms Organic 7 Grain Bread UPC 0-47593-02112-8Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
- Class II
Food Recall · December 18, 2023
RDK Corp. dba Racine Danish Kringles
Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.Raspberry Kringle may contain undeclared tree nuts (pecans).
- Class II
Food Recall · December 18, 2023
Member's Mark - Mild Cheddar Fancy (Fine) Shredded Cheese packaged in 5lbs, 8 packages per caseForeign Material - Glove remnants
- Class I
Medical Device Recall · December 18, 2023
regard Operative LAP, Item Number 800943001; surgical convenience kitSurgical convenience kits were manufactured with a component which was subsequently recalled by Nurse Assist.
- Class III
Food Recall · December 18, 2023
Shiloh Farms Organic Salt Free 7 Grain Bread UPC 0-47593-02113-5Daily recommended consumption of Cholesterol and Sodium are listed in grams instead of milligrams. Product content information is accurate.
- Class II
Food Recall · December 18, 2023
Aldi Choceur Burnt Caramel Chocolate Bars, Net Wt. 1.75oz. UPC 4099100202809Undeclared coconut
- Class II
Medical Device Recall · December 18, 2023
PulseSpray Infusion System devices including: PULSE SPRAY 5F/135/20, UPN: H787125004045, REF: 12500404; Pulse Spray 3Fx135x20, UPN: H787125004155, REF: 12500415; and PULSE SPRAY 5F/45/10, UPN: H78712Rotating adaptor O-ring manufacturing defect impacting seal integrity which may lead to a leak during infusion of medication.
- Class II
Medical Device Recall · December 18, 2023
St. Jude Medical, Atrial Fibrillation Division, Inc.
TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.When the catheters are used with the EnSiteX EP System, the system does not correctly recognize the catheter as the appropriate product model and instead reads and displays it as a different model. This results in some features specific to the catheter do not appear on the display and the catheter image may also appear inverted.
- Class II
Medical Device Recall · December 18, 2023
Vortex Surgical ACTU8 FORCEPS, 25 GA, ADAPTIVE, REF VS0740.25Reason for the voluntary recall is residue was identified on the two forceps tips of a customer in Korea. The residue is associated with one lot of forceps tips which were utilized in two lots of ACTU8 Adaptive Forceps Tips occurring in 0.25% of those lots.
- Class I
Medical Device Recall · December 15, 2023
BrightView X, gamma camera for SPECT; Model Nos.: 6-digit format 882478; 12-digit format 453560824741 453560829261;Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.
- Class II
Food Recall · December 15, 2023
Quaker Chewy Dipps Variety Pack 14ct 15 oz; 48ct 51.6 oz Bars are individually wrapped in plastic and then packaged in paperboard boxes.potential Salmonella
- Class II
Food Recall · December 15, 2023
Quaker Chewy Bars Less Sugar Variety 8ct 6.7 oz; 18ct 15.1 oz; 58ct 48.7 oz; 60ct 50.4 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes.potential Salmonella
- Class II
Food Recall · December 15, 2023
Ultimate Flavor Snack Care Package, Variety Assortment of Chips, Cookies, Crackers, & More 40ct 50.89 ozpotential Salmonella
- Class II
Food Recall · December 15, 2023
Quaker Chewy Bars Less Sugar Cookies & Cream. 1ct 1.38 oz; 8ct 6.7 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.potential Salmonella
- Class II
Food Recall · December 15, 2023
Quaker Chewy Bars S'mores 8ct 6.7 oz; 58ct 48.7 oz; 1ct 0.84 oz; 440ct 369.6 oz; 18ct 15.1 oz. Bars are individually wrapped in plastic and then packaged in paperboard boxes or totes.potential Salmonella
- Class II
Food Recall · December 15, 2023
Salted Caramel Dark Chocolate bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.Undeclared Soy Allergen in various fruit and chocolate snack bars
- Class II
Food Recall · December 15, 2023
Quaker Chewy Bars Dark Chocolate Chunk 8ct 6.7 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.potential Salmonella
- Class II
Food Recall · December 15, 2023
Quaker Chewy Granola Bars Yogurt Variety Packs 1.23 oz 10 Count; 1.23 OZ 21 Count; 41.8 oz 34 Count; 1.23 oz 14 Countpotential Salmonella
- Class II
Food Recall · December 15, 2023
Quaker Chewy Bars and Dipps Variety Pack 14ct 13 oz and 58ct 58.6 oz. Bars are individually wrapped in plastic and packaged in paperboard boxes.potential Salmonella
- Class II