Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 9,851–9,900 of 15,364
- Unclassified
Vehicle Recall · October 5, 2024
2024 BMW X5, 2025 BMW X5Incorrect tire information can allow an incorrectly sized tire to be installed or result in improperly inflated tires, increasing the risk of a crash.
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Smoke Evacuation Pencil, Coated, 70mm Blade, Push Button Switch - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke genThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Blade Push-Button - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generateThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-1.Potential failure of affected units to recharge the battery of the oxygen concentrators.
- Class II
Medical Device Recall · October 4, 2024
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.Potential failure of affected units to recharge the battery of the oxygen concentrators.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
MEDLINE INDUSTRIES, LP - Northfield
ARTHROSCOPY Convenience kit used for surgical procedures, SKU SYNJ910004CProducts within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4702Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-101.Potential failure of affected units to recharge the battery of the oxygen concentrators.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class I
Medical Device Recall · October 4, 2024
microTargeting Insertion Tube Set, P/N 66-IT-05P, Lot 244517. The intended use is to accurately guide a microelectrode or instrument in the brain during stereotactic functional neurosurgical procedureA complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of other components was included in the build order for Lot 244517 of P/N 66-IT-06P. Use of the product with a spacer tube which is too long could result in intercranial hemorrhaging and brain damage.
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke geneThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class I
Food Recall · October 4, 2024
Tipical Latin Food, Corp. dba La Pradera
Los Andes Foods Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATEDUndeclared allergen:Wheat
- Class II
Medical Device Recall · October 4, 2024
MEDLINE INDUSTRIES, LP - Northfield
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003AProducts within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Coated, 70mm - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by elThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Non-coated, 70mm - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated bThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class II
Medical Device Recall · October 4, 2024
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the needle.
- Class II
Medical Device Recall · October 4, 2024
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generaThere is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
- Class II
Medical Device Recall · October 4, 2024
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-103.Potential failure of affected units to recharge the battery of the oxygen concentrators.
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Medical Device Recall · October 3, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2) 2089507-093, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 1GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor to access the system and potentially manipulate patient data.
- Class II
Medical Device Recall · October 3, 2024
DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.
- Class II
Food Recall · October 3, 2024
Youngstown Grape Distributors, Inc.
Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingredients: Mandarin Orange, Organic Carrot Juice, Organic Pineapple Juice, Lemon Juice, and Organic Turmeric Juice. UPC 8600Incomplete pasteurization
- Class II
Medical Device Recall · October 3, 2024
Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surgeryThere is the potential for a potential sterility breach for three lots of the DLP Aortic Root Cannula due to a misaligned seal
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Food Recall · October 3, 2024
Youngstown Grape Distributors, Inc.
Farmers Juice Watermelon Hydration packaged in a 12 fl. oz. bottle; Ingredients: Watermelon, Lime, MintIncomplete pasteurization
- Class II
Medical Device Recall · October 3, 2024
DeRoyal C-SECTION TRACEPACK, REF 89-9338-06DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.
- Class II
Medical Device Recall · October 3, 2024
DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK, 89-9349-06DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Food Recall · October 3, 2024
Youngstown Grape Distributors, Inc.
Happy Moose Juice Strawberry Field packaged in a plastic 12 fl. oz. bottle. Ingredients: Organic Apple Juice, Organic Orange Juice, Organic Strawberry Puree, Organic Beet Juice, Organic Ginger Juice,Incomplete pasteurization
- Class II
Food Recall · October 3, 2024
Youngstown Grape Distributors, Inc.
Farmers Juice Carrot Digest packaged in a 12 fl. oz. bottle; Ingredients: Orange, Lemon, Carrot, Ginger, Jicama UPC: 00860006798116Incomplete pasteurization
- Class II
Medical Device Recall · October 3, 2024
DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.
- Class II
Food Recall · October 3, 2024
Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos, danes ellotes, danes cuernos, bolillos, and teleras. Bakery products are packaged in unlabeled poly bags.Undeclared allergens; wheat, soy, and eggs.
- Class II
Food Recall · October 3, 2024
Youngstown Grape Distributors, Inc.
Farmers Juice Focus Greens packaged in a 12 fl. oz. bottle; Ingredients: Cucumber, Celery, Fennel, Romaine Lettuce, Lemon, Mint, Green Cabbage, Ginger, Turmeric, Basil, & Matcha. UPC: 00860006798048Incomplete pasteurization
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Medical Device Recall · October 3, 2024
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, ItemError code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
- Class II
Food Recall · October 2, 2024
Gordon CHOICE Fruit Punch Beverage Mix Naturally and Artificially Flavored Low Calorie Instant, NET WT. 8.6 OZ (243 g), UPC 0 93901 59606 2, Case UPC 10093901596069 & NET WT. 22OZ (1 LB 6 OZ) 624 g, 0After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
- Class II
Medical Device Recall · October 2, 2024
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009The door on the Spectrum IQ Infusion pump may not be able to fully close.
- Class II
Medical Device Recall · October 2, 2024
smith&nephew LEIGON OXINIUM CONSTRAINED NONPOROUS FEMORAL COMPONENT, SIZE 3 LEFT, REF 71421163; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMERComplaint received indicating that a package contained a LGN OX CONSTRAINED FEM 3 LT implant instead of a LGN OX CONSTRAINED FEM 4 LT as described on the product label.
- Class II
Food Recall · October 2, 2024
ELLINGTON FARMS LEMONADE DRINK MIX NATURAL FLAVOR, Net Wt. 24 oz (1.5 lbs) 680g, UPC 0 46045 06155 2, Case UPC 50719098505490, Distributed by: Ben E. Keith Foods, Fort Worth, TX 76101After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.
- Class II
Food Recall · October 2, 2024
Sysco Classic Strawberry Drink Mix Artificial Flavor, NET WT. 24OZ (1 LB 8 OZ) 690g, UPC 0 74865 09328 6, Case UPC 10074865093283, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077After an investigation, the firm discovered that a sifter used in the production of the Dextrose for each product was damaged and introduced metal fragments in the products.