Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 9,651–9,700 of 15,364
- Class II
Food Recall · October 17, 2024
KODIAK CAKES 8/14.8oz GRDL WFL BLGN BTRMLK VAN-KDKCS UPC 705599014802potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
PICS BY PRICE CHOPPER 6/29.6oz GRDL WFL BB - PRCHP UPC 041735089656 NO NAME 1/1.68kg GRDL WFL BB - NNAME UPC 060383987732 NO NAME 12/280g GRDL WFL BB - NNAME UPC 060383987671 WESTERN FAMILY 12/280g GRpotential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
WEGMANS 12/13.75oz GRDL WFL BLGN CIN - WEGMN UPC 077890550014potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
COMPLIMENTS 12/390g GRDL WFL BLGN MXD BRY-CMPLM UPC 055742347180 CULINARY TOURS 12/13.75oz GRDL WFL BLGN MXD BRY - CLNTR UPC 011225148569potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
PICS BY PRICE CHOPPER 6/29.6oz GRDL WFL HSTYLE RF - PRCHP UPC 041735064912 ALWAYS SAVE 12/9.9oz GRDL WFL HSTYLE RF - ASAVE UPC 070038608752 ESSENTIALS 12/9.9oz GRDL WFL HSTYLE RF - ESSEN UPC 607880101potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
KRUSTEAZ 1/3.44lb GRDL WFL BLGN DBL CHOC-KRSTZ UPC 00041820818734 KRUSTEAZ 12/13.75oz GRDL WFL BLGN DBL CHOC-KRSTZ UPC 041820818697 GOOD & GATHER 12/13.75oz GRDL WFL BLGN DBL CHOC-GDGTR UPC 0852391579potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
DUNCAN HINES 1/3.41kg GRDL WFL BLGN 7IN-DUNHN UPC 091479060268 BAKERS SOURCE CANADA 1/3.41kg GRDL WFL BLGN 7IN - BKSCN GORDON CHOICE 1/3.41kg GRDL WFL BLGN ORIG-GDNCHpotential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
SELECTION 1/1.68kg GRDL WFL CHOC CHIP-SLCTN UPC 00059749977692 NO NAME 12/280g GRDL WFL CCH - NNAME UPC 060383987701 SELECTION 12/280g GRDL WFL CCH-SLCTN UPC 059749904711 COMPLIMENTS 12/280g GRDL WFLpotential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
SELECTION 1/1.68kg GRDL WFL ORIG-SLCTN UPC 059749904759 COMPLIMENTS 1/1.68kg GRDL WFL ORIG-CMPLM UPC 055742500530 SELECTION 12/280g GRDL WFL ORIG-SLCTN UPC 059749904704 COMPLIMENTS 12/280g GRDL WFL ORpotential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
KODIAK CAKES 8/9.88oz GRDL WFL ORIG MINI-KDKCS UPC 705599017148potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
BREAKFAST BEST 12/8 OZ GRDL HSTYLE PLNT BSD WFL-BKBST UPC 4061459885750potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
GIANT EAGLE 8/33oz GRDL PNCK BTRMLK - GT/EG UPC 030034071332 SCHNUCKS 8/33oz GRDL PNCK BTRMLK - SCHNK UPC 041318100020 SE GROCERS 8/33oz GRDL PNCK BTRMLK - SEGGR UPC 038259117170 BROOKSHIRE'S 8/33oz Gpotential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
KRUSTEAZ 12/15oz GRDL PNCK MINI BTRMLK-KTZCM UPC 686151200164potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
SIMPLE TRUTH 12/11.3oz GRDL WFL HSTYLE GF-SMPTR UPC 011110105493potential to be contaminated with Listeria monocytogenes
- Class II
Food Recall · October 17, 2024
Spice Powder, 4 oz, Plastic BagLead level was higher than NYSAGM Standard.
- Class II
Food Recall · October 17, 2024
WEGMANS 12/7.4oz GRDL WFL FLAX ORG - WEGMN UPC 077890481424 H-E-B 12/8.25oz GRDL WFL FLAX ORG-HEBUT UPC 041220708338 WEGMANS 12/8.25OZ 6CT GRDL WFL FLAX ORG-WEGMN UPC 077890577059 NATURES PATH ORGANICpotential to be contaminated with Listeria monocytogenes
- Class II
Medical Device Recall · October 17, 2024
Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, SterileA manufacturing error resulting in acceptance of valves with a leaflet deflection value that was outside of established specifications. This could potentially affect long-term durability of the impacted valve and/or cause potential valve failure.
- Class II
Medical Device Recall · October 17, 2024
Abbott Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 27 mm, NVRO-27, SterileA manufacturing error resulting in acceptance of valves with a leaflet deflection value that was outside of established specifications. This could potentially affect long-term durability of the impacted valve and/or cause potential valve failure.
- Unclassified
Consumer Product Recall · October 17, 2024
Colsen Fire Pits LLC, of Miami, Florida
Colsen-branded fire pitsAlcohol flames can be invisible and lead to flame jetting when refilling the fire pit reservoir. Flame jetting is a serious event that can occur while pouring alcohol, when fire flashes back to the alcohol container and suddenly propels burning alcohol out of the container and onto people nearby. Alcohol can also splash, spill or leak out of the fire pit reservoir during use, causing a flash fire that can spread and create larger hotter flames, that can escape the unit. Use of the recalled fire pits can lead to injury quickly and unexpectedly, causing burns in less than one second, that can be serious and deadly.
- Unclassified
Consumer Product Recall · October 17, 2024
Anker Innovations Limited, of Hong Kong, China
Anker Power BanksThe lithium-ion battery in the power banks can overheat, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · October 17, 2024
Wenzhou LingShuo Smoking Accessories Co. Ltd., of China
Nub, Serie V, Cain, and Oliva branded Promotional Cigar Slim LightersThe recalled lighters do not have child-resistant mechanisms and were not tested to the federal regulatory requirements for child resistance. Young children under 5 years of age could ignite the lighters, posing fire and burn hazards.
- Class I
Medical Device Recall · October 16, 2024
Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is Vantive.Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
- Class II
Medical Device Recall · October 16, 2024
Smaxel Fractional CO2 Laser, a Class IV medical laser system.The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter ConnectorThe connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000ZDeviations in the manufacturing process created a compromise in the sterile barrier, in which sterility cannot be assured during the duration of the product's 2-year shelf life.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268B; 2) COMBINED SPINAL AND EPIDURAL, REF DYNJRA1268C; 3) FEMORAL BLOCK TRAY, REF DYNJRA1739A; 4) FEMORThe connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699; 2) L&D CONTINUOUS EPIDURAL TRAY, REF PAIN1699AThe connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Food Recall · October 16, 2024
Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray Net wt. variable - average 1.52 lbs. UPC 00226529000004, UPC 00409802813793Presence of Listeria monocytogenes
- Class II
Medical Device Recall · October 16, 2024
Acrobat-i Positioner. Model Number C-XP-5000ZDeviations in the manufacturing process created a compromise in the sterile barrier, in which sterility cannot be assured during the duration of the product's 2-year shelf life.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876AThe connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023; 4) TRAY, CONT EPI 20G NYL W/ HUST,The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622AThe connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class II
Medical Device Recall · October 16, 2024
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000ZDeviations in the manufacturing process created a compromise in the sterile barrier, in which sterility cannot be assured during the duration of the product's 2-year shelf life.
- Class II
Medical Device Recall · October 16, 2024
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX onlyRetroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence.
- Class II
Medical Device Recall · October 16, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF PAIN1644The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
- Class III
Medical Device Recall · October 15, 2024
a) Alcon Custom-Pak CONSTELLATION 25G PLUS CHRISTIANA CARE HLTH SERV, # 15340-11, containing TUBING, SALEM SUMP, 14 FR; b) Alcon Custom-Pak DR GREEN VITRECTOMY MERCY HOSPITAL, # 6557-59 and # 6557Reported breakage in the tubing Anti-Reflux Valve (ARV) due to improper use. As a result, changes to labeling were made.
- Class II
Medical Device Recall · October 15, 2024
Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile, femoral head bipolar component of the Tandem Bipolar Hip System.The Bipolar assembly contains an oversized Retainer Ring.
- Class II
Food Recall · October 15, 2024
All Raw Vegan Certified Organic Salsa, Glaser Organic Farms, Handmade fresh from our farm to you,Net wt. 8 oz, Plastic PET Container with cover, Keep Refrigerated, UPC 832910 001514Product may contain Foreign object: Glass
- Class I
Medical Device Recall · October 15, 2024
Brand Name: Atlan Product Name: Atlan A300 Model/Catalog Number: 8211300 The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates.The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class I
Medical Device Recall · October 15, 2024
Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Component: Not applicableThe Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class II
Medical Device Recall · October 15, 2024
OrganOx metra -Intended as a Normothermic Machine Perfusion system of donor transport livers. Model/Catalog Number: D0003 The OrganOx metra is a transportable device intended to be used to sustaBattery movement led to damage of one of the battery cells causing it to short to the battery retention bracket
- Class I
Medical Device Recall · October 15, 2024
Brand Name: Atlan Product Name: Atlan A300XL Model/Catalog Number: 8621400 The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates.The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class II
Medical Device Recall · October 15, 2024
MEDLINE INDUSTRIES, LP - Northfield
(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
- Class I
Medical Device Recall · October 15, 2024
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicableThe Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- Class II
Medical Device Recall · October 15, 2024
MEDLINE INDUSTRIES, LP - Northfield
(1) Medline Pacer Implant Pack, REF DYNJ59194A, 4 kits/case, sterile; and (2) Medline Thoracotomy Morristown, REF DYNJ904220F, 1 kit/case, non-sterile.Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
- Class II
Medical Device Recall · October 15, 2024
MEDLINE INDUSTRIES, LP - Northfield
Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
- Class II
Medical Device Recall · October 14, 2024
Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiacWithin the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient
- Class II
Medical Device Recall · October 14, 2024
Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.)Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient