Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,261 results
Food & Beverage
RappelConsoGeneral Alert

citroen - spacetourer, jumpy fourgonnette / véhicule utilitaire léger

le corps du démarreur peut entrer en contact avec le câble positif de la batterie en raison d’une protection insuffisante du câble. cela pourrait provoquer un arc électrique ou un court-circuit, conduisant à la fumée du compartiment moteur et à un incendie.

Jul 2, 2026citroen
Safety Alert
Health CanadaType II

Glidesheath Slender® Introducer Sheath

Performance

Jul 2, 2026Medical devices
AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suff...
CPSCGeneral Alert

AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suff...

The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows?and infant support cushions because they can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation.

Jul 2, 2026
Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fir...
CPSCGeneral Alert

Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fir...

The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.

Jul 2, 2026Cooper Lighting, LLC, of Peachtree City, Georgia
Vehicle
NHTSAFUEL SYSTEM, GA...

Crestline Coach Ltd. - Park Outside: Fuel Line May Leak and Cause Fire

A fuel leak increases the risk of a fire.

Jul 2, 2026Crestline Coach Ltd.
Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
CPSCGeneral Alert

Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

Jul 2, 2026
Safety Alert
Health CanadaType II

WASPLab

Performance

Jul 2, 2026Medical devices
Medical Device
FDA DevicesClass I

Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC01...

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.

Jul 1, 2026Medline Industries, LP
Vehicle
NHTSASTRUCTURE

Honda (American Honda Motor Co.) - Improperly Tightened Rear Subframe Bolts

Loose rear subframe bolts can lead to a loss of vehicle stability or rear subframe detachment, increasing the risk of a crash or injury.

Jul 1, 2026Honda (American Honda Motor Co.)
Neon wall lamp
Australia ProductsButton batteries

Neon wall lamp

The product doesn’t comply with the mandatory standards for products containing button/coin batteries . The product was not tested prior to sale and is missing warning information about the dangers of button/coin batteries to children what to do when a person suspects someone has swallowed or placed a button/coin battery inside any part of their body.

Jul 1, 2026
Vehicle
NHTSAGeneral Alert

BMW of North America, LLC - Integrated Brake System Malfunction

A loss of power brake assist can extend the distance required to stop the vehicle. Additionally, malfunctioning ABS and/or DSC systems can cause a loss of vehicle control. Either of these scenarios can increase the risk of a crash.

Jul 1, 2026BMW of North America, LLC
Medical Device
FDA DevicesClass II

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, b...

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

Jul 1, 2026SURGIFY MEDICAL OY
Vehicle
NHTSAEXTERIOR LIGHTING

Chrysler (FCA US, LLC) - Parking & Daytime Running Lights May Fail/FMVSS 108

Parking lights and daytime running lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.

Jul 1, 2026Chrysler (FCA US, LLC)
Medical Device
FDA DevicesClass I

Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Pro...

Potential for thrombus formation during prolonged use of the introducer.

Jul 1, 2026Abiomed, Inc.
Medical Device
FDA DevicesClass II

Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide ...

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Jul 1, 2026Zimmer, Inc.
Food & Beverage
FDA FoodClass I

1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.

Potential presence of Salmonella.

Jul 1, 2026Utz Quality Foods, LLC
Food & Beverage
FDA FoodClass I

Spring & Mulberry Pecan Date Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), in...

Potential Salmonella contamination.

Jul 1, 2026Spring & Mulberry Inc.
Medical Device
FDA DevicesClass II

Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ ...

Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.

Jul 1, 2026Zimmer, Inc.
Medical Device
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ...

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

Jul 1, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ...

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

Jul 1, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Num...

Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage.

Jul 1, 2026Zimmer, Inc.
Pharmaceutical
FDA DrugsClass II

DULOXETINE D/R, a) 30 mg (NDC 61919-482-30), 30 Caps; b) 30 mg (NDC 61919-482-60...

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit

Jul 1, 2026Direct Rx
Pharmaceutical
FDA DrugsClass II

Povi-One, 10% Povidone-Iodine Oral Antiseptic, Packaged by Elevate Oral Care, LL...

sub potency

Jul 1, 2026Elevate Oral Care
les moulinettes - fusilli epeautre
RappelConsovolontaire (san...

les moulinettes - fusilli epeautre

taux de t-2 toxine et ht-2 toxine supérieures à la valeur réglementaire

Jul 1, 2026les moulinettes
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