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Found 28,896 results for "recall check"

Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY, D AND C PACK, MAD D & C, VPH LITHOTOMY MINOR, TRMC- PERI GYN PACK, RICH MINOR LITHOTOMY, etc. (see recall documents for a full list of products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: KIT URO ROBOT CYSTECTOMY, D AND C PACK, MAD D & C, VPH LITHOTOMY MINOR, TRMC- PERI GYN PACK, RICH MINOR LITHOTOMY, etc. (see recall documents for a full list of products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as BASIC GYN, CW LAP GYN, D&C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP PACK, FLOYD LAP GYN, GYN LAP PACK, GYN LAPAROSCOPY, GYN MINOR PACK, etc. (see the recall documents for a full list of affected products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as BASIC GYN, CW LAP GYN, D&C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP PACK, FLOYD LAP GYN, GYN LAP PACK, GYN LAPAROSCOPY, GYN MINOR PACK, etc. (see the recall documents for a full list of affected products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Safety AlertCanadaHealth Canada

Izem Energy brand “Boisson énergisante gazeuse” recalled due to labelling issues

CFIA
Health CanadaClass 2

Izem Energy brand “Boisson énergisante gazeuse” recalled due to labelling issues

Labelling and packaging

Jun 24, 2026CFIA
Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, ASC T&A, CONWAY T&A SINUS, EAR PACK, etc. (see the recall documents for the full list of products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: ADULT TRACHEOSTOMY TUBE INSERT, ASC T&A, CONWAY T&A SINUS, EAR PACK, etc. (see the recall documents for the full list of products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cystectomy, etc. (see the recall documents for a full list of products)

Medline Industries, LP
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cystectomy, etc. (see the recall documents for a full list of products)

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Food & BeverageUKUK FSA

Morrisons recalls Morrisons Coronation Chicken Pasta because of undeclared milk

Morrisons
UK FSAPublished

Morrisons recalls Morrisons Coronation Chicken Pasta because of undeclared milk

Milk This product may contain milk making it a possible health risk for anyone with an allergy to milk or intolerance to milk or milk constituents.

Jun 24, 2026Morrisons
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026302 - GENERAL MOTORS

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026302 - GENERAL MOTORS

Seats And Restraints

Jun 23, 2026TC
Food & BeverageUKUK FSA

Prepworld recalls fruit products because of possible contamination with Salmonella

Prepworld
UK FSAPublished

Prepworld recalls fruit products because of possible contamination with Salmonella

The possible presence of Salmonella in the products listed above. Symptoms caused by Salmonella usually include fever, diarrhoea and abdominal cramps. If you are experiencing these symptoms, you should stay away from work, school or nursery until you have stopped having symptoms for at least 48 hours to avoid passing it on to others.

Jun 23, 2026Prepworld
Safety AlertCanadaHealth Canada

Portable Hook-On Chair recalled due to fall hazard

Consumer product safety
Health CanadaGeneral Alert

Portable Hook-On Chair recalled due to fall hazard

Fall hazard

Jun 22, 2026Consumer product safety
Food & BeverageUKUK FSA

Krispy Kreme recalls Individual Pitch Perfect Doughnut & Match Day Dozen because of undeclared hazelnuts (nuts)

Krispy Kreme
UK FSAPublished

Krispy Kreme recalls Individual Pitch Perfect Doughnut & Match Day Dozen because of undeclared hazelnuts (nuts)

Hazelnuts (nuts) These products may contain hazelnuts (nuts) making it a possible health risk for anyone with an allergy to hazelnuts (nuts).

Jun 21, 2026Krispy Kreme
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026279 - FORD

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026279 - FORD

Other

Jun 19, 2026TC
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026286 - FORD

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026286 - FORD

Lights And Instruments

Jun 19, 2026TC
Safety AlertCanadaHealth Canada

Wu Xian Zhai brand Soybean Snacks recalled due to undeclared wheat and / or egg

CFIA
Health CanadaClass 1

Wu Xian Zhai brand Soybean Snacks recalled due to undeclared wheat and / or egg

Egg - Wheat - Gluten

Jun 19, 2026CFIA
Food & BeverageUKUK FSA

Traditional Cheese Company recalls French Bries because of contamination with Listeria monocytogenes

Traditional Cheese Company
UK FSAPublished

Traditional Cheese Company recalls French Bries because of contamination with Listeria monocytogenes

The presence of Listeria monocytogenes in the products listed above. Symptoms caused by Listeria monocytogenes can be similar to flu and include high temperature, muscle ache or pain, chills, feeling or being sick and diarrhoea. However, in rare cases, the infection can be more severe, causing serious complications, such as meningitis. Some people are more vulnerable to listeria infections, including those over 65 years of age, pregnant women and their unborn babies, babies less than one month old and people with weakened immune systems.

Jun 19, 2026Traditional Cheese Company
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026238 - HYUNDAI

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026238 - HYUNDAI

Other

Jun 19, 2026TC
Safety AlertUSCPSC

Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products

Unknown Firm
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products
CPSCGeneral Alert

Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products

The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's thickness exceeds the maximum limit, posing a suffocation hazard; and an infant could fall out of an enclosed opening at the foot of the lounger or become entrapped. The portable loungers do not have a stand, posing a fall hazard. These violations create an unsafe sleeping environment for infants, posing a risk of serious injury or death.

Jun 18, 2026
Safety AlertCanadaHealth Canada

Transport Canada Recall - 2026241 - TOYOTA

TC
Health CanadaGeneral Alert

Transport Canada Recall - 2026241 - TOYOTA

Engine

Jun 18, 2026TC
Safety AlertUSRSS Feed

Clover Hill Dairy Expands Recall to Include All Clover Hill Dairy Brand Cheese Due to Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Clover Hill Dairy Expands Recall to Include All Clover Hill Dairy Brand Cheese Due to Possible Health Risk

Jun 18, 2026
Safety AlertCanadaHealth Canada

Joolz Aer2 Car Seat Adapter Set recalled due to fall hazard

Consumer product safety
Health CanadaGeneral Alert

Joolz Aer2 Car Seat Adapter Set recalled due to fall hazard

Fall hazard

Jun 18, 2026Consumer product safety
Safety AlertUSCPSC

GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys

Unknown Firm
GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
CPSCGeneral Alert

GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys

The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's throat and become lodged, posing a serious risk of respiratory distress and deadly choking hazard.

Jun 18, 2026
Safety AlertUSCPSC

Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear

Unknown Firm
Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear
CPSCGeneral Alert

Veseacky Pajama Sets Recalled Due to Risk of Serious Injury Death from Burn Hazard; Violate Mandatory Standards for Children's Sleepwear

The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.

Jun 18, 2026
Safety AlertUSCPSC

Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban

Unknown Firm
Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban
CPSCGeneral Alert

Bada Boom Fireworks Recalls Pyro Diablo "Diablo Rising" Fireworks Due to Risk of Serious Injury or Death from Explosion and Burn Hazards; Violate Fireworks Ban

The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that exceeds the federal limit, posing deadly explosion and burn hazards. Overloaded fireworks can result in a greater than expected explosion.

Jun 18, 2026
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