Safety Recalls

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15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.

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Showing 13,501–13,550 of 15,379

Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT, Product Code 65340; b) STERILE CURV MOSQUITO HEMOSTAT (MHS103), Product Code 66145; c) STERILE STRT KELLY HEMOSTAT (SK8039), P
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE SWABSTICKS PVP 3 PK, Product Code DYNDA2724
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE M1S0179 STRL TAPE/PEN PACK, Product Code P519582A
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion STERILE #16 RUBBER BAND, Product Code EB16
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
CareFusion 303, Inc.
BD Pyxis MedStation Auxiliary 4000 REF: 306. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion STERILE BLOOD COLLECTION TUBE,10ML, Product Code 6430ST
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE, Product Code 66825; b) STERILE PAS #3 BLADE HANDLE (BH3PAS), Product Code I68290
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
Siemens Medical Solutions USA, Inc.
ACUSON Juniper Diagnostic Ultrasound System, REF: 11335791, and ACUSON Juniper Select Diagnostic Ultrasound System, REF: 11653093, running software version VA10x with DICOM SR Cardiac option, from VB1
On ultrasound systems, when Cardiac DICOM SR feature is configured to display either minimum or maximum measured value, and multiple cardiac region measurements are made, and results are exported into the SR feature, then The SR viewer will display the LAST measured value, not min or max, which could contribute to patient condition misdiagnosis or negatively influence patient management decisions.
Class II
Medical Device Recall · February 23, 2024
Siemens Medical Solutions USA, Inc.
ACUSON Redwood 1.0 Diagnostic Ultrasound System, REF: 11503314, running software version VA10A to VA10G
On ultrasound systems, when Cardiac DICOM SR feature is configured to display either minimum or maximum measured value, and multiple cardiac region measurements are made, and results are exported into the SR feature, then The SR viewer will display the LAST measured value, not min or max, which could contribute to patient condition misdiagnosis or negatively influence patient management decisions.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Curette kits labeled as: a) STERILE BUCK EAR CURETTE "00" (25697), Product Code 66745; b) STERILE "1" EAR CURETTE (505629), Product Code 67050; c) STERILE FOX DERMAL CURETTE, 5MM(32923
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
CareFusion 303, Inc.
BD Pyxis MedStation Auxiliary ES REF: 324. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Class II
Medical Device Recall · February 23, 2024
Human Care Hc Sweden Ab
Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141), Product Code 66165; b) STERILE WEBSTER NEEDLEHOLDER, Product Code 66185; c) STERILE ADSON FORCEP SERR (598), Product Code
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE 4.5 IN WIRE CUT SCISSORS, Product Code DYND04006
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
CareFusion 303, Inc.
BD Pyxis MedStation ES (Med ES Main) REF: 323. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion manual surgical kits labeled as: a) SUTURE REMOVAL TRAY, Product Code TRI55405; b) SUTURE REMOVAL SET, Product Code 60265 MEDLINE manual surgical kits labeled as: a) SUTURE REMOVAL
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Manual surgical kits labeled as: a) HEGAR UTERINE DILATOR, 11-12MM, STERILE, Product Code HUD112ST; b) STERILE UTERINE DILATOR 1MM/2MM, Product Code HUD12ST; c) HEGAR UTERINE DILATOR,
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173), Product Code 66520; b) STERILE TOWEL CLAMP, Product Code A547ST; c) ST TOWEL CLAMPS NON PERFORATING (P/S), Product Code
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
Agfa N.V.
Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generat
Steel cable installed inside the mobile column which supports the weight of the telescopic arm with the tube head has potential risk -an interference could cause the safety system which blocks the arm if the cable is cut off does not work properly, may result in patient injury
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion retractor kits labeled as: a) STERILE 6-1/2" SENN RETRACTOR (ST7185), Product Code 66795; b) STERILE RAGNELL RETRACTOR (RR602), Product Code 67525; c) ST. SENN RETRACTOR 3 PRG BLUNT (ST
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion PICC LINE SECUREMENT KIT, Product Code IVS565
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP, Product Code 15MLVLCP; b) STERILE 9X12 RECLOSABLE BAG, Product Code MG912ST
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion STERILE TRACH BRUSH, Product Code 6225ST
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
RAYSEARCH LABORATORIES AB
RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B, 2024A including some service packs.
A use error that has occurred with RayStation/RayPlan, where material override using Silicon, Si, was incorrectly selected for a silicone gel polymer implant.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion kits: a) DENTAL INSTRUMENT KIT, Product Code DH760; b) STERILE COTTON DENTAL ROLLS 6/PK, Product Code 9125ST6; c) DENTAL INSTRUMENT KIT, Product Code DH760
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Food Recall · February 23, 2024
Backstage Center DBA CTC Seller
Alipotec Raiz de Tejocote dietary supplements, Net. Wt. 0.35oz, plastic bottle labeled with the "Alipotec King" sticker. Store at room temperature.
The "Alipotec King" Alipotec Raiz de Tejocote product was found to contain toxic yellow oleander instead of tejocote.
Class I
Medical Device Recall · February 23, 2024
CareFusion 303, Inc.
BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
MEDLINE SWABSTICKS ALCOHOL 3PK, Product code DYNDA2723
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10", Product Code I68905; b) VAGINAL REPAIR KIT, Product Code MNS11505; c) PTCA ADD-ON KIT, Product Code MNS11545; d) INSTR
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion STERILE #5 LARYNGEAL MIRROR(505709), Product Code 67830
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Medical Device Recall · February 23, 2024
Magellan Diagnostics, Inc.
The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors
Calibration Buttons being used in the kitting process were incorrectly labeled as Lot 2323M for lot 2333M. The use of mislabeled calibration Button with Lot #2333 can lead to delayed or erroneous high or erroneous low results.
Class II
Medical Device Recall · February 23, 2024
MEDLINE INDUSTRIES, LP - Northfield
Centurion FCP MAGILL CATH 7.5 IN PED (67575), Product Code 67575
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
Class II
Consumer Product Recall · February 22, 2024
Worthington Enterprises, of Columbus, Ohio
EVAS 20-lb. propane exchange cylinders
The recalled propane exchange cylinders could leak gas, posing a fire hazard.
Unclassified
Consumer Product Recall · February 22, 2024
Hangzhou Sharejoy Ecommerce Co. Ltd, dba Biloban, of China
Spring Spirit and Biloban Pack and Play Mattresses
The recalled mattresses violate multiple provisions of the federal safety regulation for crib mattresses, including the thickness test, and are missing warnings and labels. The product poses a suffocation hazard to infants.
Unclassified
Consumer Product Recall · February 22, 2024
IKEA Supply AG, of Switzerland
ÅSKSTORM 40W USB Chargers
The USB charger's cable can become damaged or break over time, posing burn and electric shock hazards.
Unclassified
Medical Device Recall · February 22, 2024
Baxter Healthcare Corporation
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specia
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Class II
Medical Device Recall · February 22, 2024
Baxter Healthcare Corporation
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specia
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Class II
Drug Recall · February 22, 2024
Eugia US LLC
Tobramycin for Injection, USP, 1.2 grams per Pharmacy Bulk Package, Rx Only, For Intravenous Use, PHARMACY BULK PACKAGE NOT FOR DIRECT INFUSION, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520,
Failed Stability Specification: Water determination was found not complying with specification.
Class II
Medical Device Recall · February 22, 2024
Bolton Medical Inc.
RELAY PRO Thoracic Stent-Graft System, containing one endovascular stent-graft system, IFU, and patient tracking card, sterile: (a) Part number 28-M4-34-100-34U; (b) Part number 28-M4-30-095-30U;
The stent-graft inside the delivery system was the incorrect size.
Class II
Food Recall · February 22, 2024
Barsotti Juice Company, Inc.
Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bottles Perishable, Keep Refrigerated Ingredient: Fresh Pressed Organic Carrot Juice. Flash Pasteurized. Barsotti Juice Co., Camino, CA 95709
Product was determined to be under processed.
Class II
Consumer Product Recall · February 22, 2024
Kaka Trading Co. LTD, of China
JURLEA Area Rugs
The rugs violate the federal flammability regulations for carpets and rugs, posing a fire hazard.
Unclassified
Medical Device Recall · February 22, 2024
Baxter Healthcare Corporation
Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specia
The Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe Intravascular Probe contain inaccurate content that does not align with the products Instructions for Use (IFU).
Class II
Consumer Product Recall · February 22, 2024
Jomani International Inc., of Monterey Park, California
MouTec brand Biometric Firearm Safes
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
Unclassified
Consumer Product Recall · February 22, 2024
Cascade Designs Inc., of Seattle, Washington
MSR camping cooking pots
The pot handle can detach or become loose, posing burn and scald risks to consumers from hot food and liquids spilling from the product.
Unclassified
Consumer Product Recall · February 22, 2024
Shenghaina Technology Co. Ltd., d/b/a Awesafe, of China
Awesafe Biometric Gun Safes
The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death.
Unclassified
Consumer Product Recall · February 22, 2024
Bulldog Cases, of Danville, Virginia
Bulldog Biometric Firearm Safes
The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death if the safe is used to store firearms.
Unclassified
Consumer Product Recall · February 22, 2024
Machir LLC, of Springfield, Missouri
Machir Biometric Personal Safes
The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death if the safe is used to store firearms.
Unclassified
Consumer Product Recall · February 22, 2024
Magik & Kover, of China
Magik & Kover Pack and Play Mattresses
The recalled mattresses violate multiple provisions of the federal safety regulation for crib mattresses, including the thickness test, and are missing warnings and labels. The product poses a suffocation hazard to infants.
Unclassified
Consumer Product Recall · February 22, 2024
Polaris Industries Inc., of Medina, Minnesota
Model Year 2022-2024 MATRYX Snowmobiles equipped with PATRIOT 650 and 850 Engines
The primary (drive) clutch can fail causing the clutch or its components to separate from the vehicle, posing an injury hazard.
Unclassified
Medical Device Recall · February 21, 2024
Bruder Healthcare Company, LLC
Thermalon Stye Compress, Item Number 24352
Thermalon and MediBeads moist heat compresses from certain lots may have been exposed to excessive moisture, resulting in potential growth of mold and/or mildew.
Class II