Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,001–11,050 of 15,364
- Class I
Food Recall · July 19, 2024
Freshire Farms - Green Beans packaged in plastic bags at 1lb, 14 bags per casePotential contamination with Listeria monocyotgenes
- Class I
Food Recall · July 19, 2024
GBC Food Services, LLC dba Yummi Sushi
Supreme Grilling Veggies 8-50053-68584 19 OZ Supreme Vegetable Kabobs 8-50053-68585 27 OZ Supreme Vegetable Bowl 8-60010-50713 26 OZpossible contamination with Listeria Monocytogenes.
- Class I
Food Recall · July 19, 2024
Freshire Farms - Jalapenos packaged in plastic bags at 8oz, 18 bags per casePotential contamination with Listeria monocyotgenes
- Class II
Food Recall · July 19, 2024
Pita Jungle Hummus & Pita Chips packaged as individual "snack pack" in 9.2oz clamshell plastic container.Finished product label does not declare sesame which is an ingredient of hummus (tahini).
- Class I
Food Recall · July 19, 2024
GBC Food Services, LLC dba Yummi Sushi
Supreme Peppers Tri Blend 8-50053-68534 8 OZ Supreme Jalapenos Diced 8-50053-68536 7 OZ Supreme Peppers W/Onions 8-50053-68538 7 OZ Supreme Peppers Snacking 8-50053-68553 12 OZpossible contamination with Listeria Monocytogenes.
- Class III
Food Recall · July 19, 2024
Almond Croissant in a clear plastic bag with a white paper label attached to the top of the plastic bag.Finished product label stated almond in the product name but did not declare tree nuts or almonds in the ingredients or allergen statement.
- Class I
Food Recall · July 19, 2024
Butternut Squash Cubes - 12oz Plastic Clam-Shell ContainerListeria monocytogenes
- Class I
Food Recall · July 19, 2024
Freshire Farms - Green Peppers packaged in plastic bags containing 3 peppers, 16 bags per casePotential contamination with Listeria monocyotgenes
- Class I
Food Recall · July 19, 2024
Salsa Medium - 16 oz Salsa Mild - 16 oz Plastic Clam-Shell ContainerListeria monocytogenes
- Class II
Food Recall · July 19, 2024
Pita Jungle Greek Salad packaged in 11.8oz plastic clamshell container.Finished product label stated feta but did not declare milk in the sub-ingredients or allergen statement.
- Class I
Food Recall · July 19, 2024
Poblano packaged as 5lb half sliced with 2 bags per case, 5lb fourth diced with 2 bags per case, 5lb half diced with 2 bags per casePotential contamination with Listeria monocyotgenes
- Class II
Food Recall · July 19, 2024
Apple Danish in a clear plastic bag with a white paper label attached to the top of the plastic bag.Allergens were declared but the finished product label incorrectly listed ingredients of Almond Croissant.
- Class I
Food Recall · July 19, 2024
Jalapeno peppers packaged as 5lb diced with 2 bags per case, whole as 10lb carton, or whole as 5lb cartonPotential contamination with Listeria monocyotgenes
- Class I
Medical Device Recall · July 19, 2024
ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011Thrombectomy system catheter instructions for use updated to reduce adverse events due to the following circumstances: 1) Fibrous, firmly adherent, calcified material, or suspected tumor thrombus overloading catheter bag 2) Catheter pulled through internal jugular vein access site or not pulled away from heart; may lead to device entrapment, pulmonary embolism, venous cutdown, abdominal surgery.
- Class II
Medical Device Recall · July 18, 2024
Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of the urinary tract.There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Class II
Medical Device Recall · July 18, 2024
smiths medical portex, 'ORATOR' SPEAKING VALVE FOR TRACHEOSTOMY TUBE, REF 100/550/000Uncertainty in the seal integrity of the sterile packaging.
- Class II
Medical Device Recall · July 18, 2024
vanSonnenberg Sump Locking Pigtail Regular Kit Sump Catheter System Kit, Material Number REF M001273090; for use as a percutaneously placed drain for intra-abdominal fluid collections.There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Class II
Medical Device Recall · July 18, 2024
smiths medical portex, Y' PIECE 15MM, REF 100/276/000Uncertainty in the seal integrity of the sterile packaging.
- Class II
Medical Device Recall · July 18, 2024
prodisc C SK, Total cervical disc replacement, medical device, Model/Catalog Number: PDSM5During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
- Class II
Medical Device Recall · July 18, 2024
Flexima Regular Kit Biliary Catheter System Kit, Material Numbers REF M001271650; bile drainage catheter with locking pigtailThere is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Class I
Drug Recall · July 18, 2024
Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
- Class II
Medical Device Recall · July 18, 2024
Flexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF M001271960, b) REF M001271970; all-purpose drainage catheter with locking pigtailThere is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Class II
Medical Device Recall · July 18, 2024
smiths medical portex, 15mm Double Swivel Connector: a) REF 100/255/150; b) REF 100/255/150JP; c) REF 100/255/150 JSUncertainty in the seal integrity of the sterile packaging.
- Class II
Medical Device Recall · July 18, 2024
prodisc C SK, Total cervical disc replacement, Model/Catalog Number: PDSM5During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
- Class III
Drug Recall · July 18, 2024
Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra Strength, Rapid Release Gelcaps, packaged in a 225-count HDPE bottle, further packaged in a carton, Distributed by Walgreen Co., 200 WilmotLabel mix-up: Carton incorrectly labeled.
- Class II
Medical Device Recall · July 18, 2024
VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the urinary tract.There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Class II
Drug Recall · July 18, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New JerseDefective container; yellow colored spike from cap lodged in the nozzle
- Class II
Medical Device Recall · July 18, 2024
smiths medical portex, Nasopharyngeal Airway, Sizes as follows: a) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060; b) AIRWAY NASOPHARYNGEAL 6.0MM, REF 100/210/060JP; c) AIRWAY NASOPHARYNGEAL 7.0MUncertainty in the seal integrity of the sterile packaging.
- Class II
Medical Device Recall · July 18, 2024
smiths medical portex, Thermovent 1200, 15mm/22mm: a) REF 100/582/000; b) REF 100/582/000JP; c) REF 100/582/000JSUncertainty in the seal integrity of the sterile packaging.
- Class II
Medical Device Recall · July 18, 2024
BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA) Catalog Number: 245128May intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of Mycobacterium tuberculosis isolates.
- Unclassified
Consumer Product Recall · July 18, 2024
BISSELL Homecare Inc., of Grand Rapids, Michigan
BISSELL® Steam Shot™ Handheld Steam CleanersThe recalled steam cleaners can expel hot water or steam onto users while heating or during use, posing a burn hazard.
- Unclassified
Consumer Product Recall · July 18, 2024
Sassy Baby Inc., of Gonzales, Louisiana
Brilliant Bee RattlesThe wooden base can detach from the wooden rod and release the three plastic rings, posing a choking hazard to young children.
- Unclassified
Consumer Product Recall · July 18, 2024
CFMOTO Powersports Inc., of Plymouth, Minnesota
CFMOTO ZFORCE 950 HO Sport Side-by-Side ROVs (2022-2023)The shock absorber rod assembly can unthread and detach, causing suspension collapse, posing crash and tip-over hazards to the rider.
- Class II
Medical Device Recall · July 17, 2024
Boston Scientific Neuromodulation Corporation
WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset, which may lead to transient loss of stimulation; patients may experience undesired sensations when therapy turns off for approx. 10-15 seconds and then back on, which may lead patient to request surgical intervention for replacement or revision.
- Class I
Food Recall · July 17, 2024
Kenny's Farmhouse Cheese - St. Jerome packaged in plastic vacuum sealed bags in 7oz wedges and whole 15lb wheelsPotential contamination with Listeria monocytogenes
- Class II
Medical Device Recall · July 17, 2024
Beckman Coulter Biomedical GmbH
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
- Class II
Medical Device Recall · July 17, 2024
Beckman Coulter Biomedical GmbH
Power Express, REF B90918The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
- Class II
Medical Device Recall · July 17, 2024
Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (Spectrum IQ infusion pump)The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.
- Class II
Medical Device Recall · July 17, 2024
Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pump) or 3570009 (Spectrum IQ infusion pump) Baxter SIGMA SpecThe Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.
- Class II
Medical Device Recall · July 17, 2024
Beckman Coulter Biomedical GmbH
PE Centrifuge, REF: B36365, a component of the Power ExpressThe adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
- Class II
Medical Device Recall · July 17, 2024
Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrumentSoftware anomalies which can result in two separate issues: A lagging screen display during a navigated procedure; or the potential for a mismatch between the navigated screw and the screw information presented on the screen.
- Class III
Medical Device Recall · July 16, 2024
Beckman Coulter IRISPEC CA/CB/CC Urine Chemistry Controls, Catalog Number REF 800-7211 and 800-7702, in vitro diagnostic device.Beckman Coulter has become aware of an increase in customer complaints for intermittent IRISpec CB negative glucose control failure, resulting in false positive control results when used in conjunction with iChemVELOCITY Urine Chemistry Strips (PNs 800-7204 and 800-7212) on the iChemVELOCITY Analyzer. This issue may delay the reporting of patient results, with a worst-case scenario of a delay in diagnosis or treatment of metabolic disorders, kidney function abnormalities, urinary tract infections, and liver function.
- Class I
Medical Device Recall · July 16, 2024
CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of the following CADD Solis Ambulatory Infusion Systems: 21-2101-0100-50, 21-2101-0200-02, 21-2101-020Damage to the battery pack may have caused a short to a capacitor within the battery pack. While the battery encasement is designed to be flame retardant, a short to the capacitor could lead to melting of the battery pack case. If this issue occurs, the battery pack charging circuit may become inoperable.
- Class I
Medical Device Recall · July 16, 2024
Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo, O2, Brazil EV300; CA2200X12B Trilogy Evo, O2, Canada EV300; DE2200X13B TriFirm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.
- Class I
Medical Device Recall · July 16, 2024
Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil CA2110X12B Trilogy Evo, Canada DE2100X13B TrilogyFirm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.
- Class I
Medical Device Recall · July 16, 2024
Trilogy Evo Universal Ventilator, Model No. DS2000X11BFirm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.
- Class II
Medical Device Recall · July 15, 2024
Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB,2.4 Model/Catalog Number: 8065772465 Software Version: N/A Product Description: Ophthalmic knife Component: N/AAlcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
- Class II
Medical Device Recall · July 15, 2024
Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106 Software Version: N/A Component: N/AAlcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
- Class II
Medical Device Recall · July 15, 2024
Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog Number: 8065992445 Software Version: N/A Product Description: Ophthalmic knife Component: N/AAlcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.
- Class II
Medical Device Recall · July 15, 2024
Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Model/Catalog Number: 8065911901 Software Version: N/A Product Description: Ophthalmic knife Component: N/AAlcon has detected an increase in complaint reports related to sharpness for specific ClearCut Dual Bevel Sideport and A-OK Comeal/Scleral V-Lance Ophthalmic knives.