Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,372 results
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Nu...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog ...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) CVC PACK, Model Number: CVI4500A; 2) TOTE KAMAL ...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Food & Beverage
FDA FoodClass II

Loard's Banana Ice Cream - 32 oz; 56 oz

Undeclared Milk, Yellow #5.

May 13, 2026Silver Moon LP dba Loard's Ice Cream
Food & Beverage
FDA FoodClass II

Lemon Creamed Honey, 671333101353 *These product labels may also say Whipped Ho...

Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

May 13, 2026Walker Honey Co
Vehicle
NHTSASTRUCTURE

Hiab USA Inc. - Liftgate Deck Pins May Break

A liftgate that falls unexpectedly increases the risk of injury.

May 13, 2026Hiab USA Inc.
Food & Beverage
FDA FoodClass II

Loard's Mango Ice Cream - 32 oz; 56 oz

Undeclared Milk, Yellow #5.

May 13, 2026Silver Moon LP dba Loard's Ice Cream
Food & Beverage
FDA FoodClass II

Loard's Egg Nog Ice Cream - 32 oz

Undeclared Milk, Eggs, Yellow #5.

May 13, 2026Silver Moon LP dba Loard's Ice Cream
Medical Device
FDA DevicesClass II

LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUD...

For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhythmia and Pause (M312 only). In addition, for these devices that are not being monitored, the LATITUDE Clarity programming screens have discrepant information, indicating that the monitoring is enabled for these features in one location and not enabled in another location.

May 13, 2026Boston Scientific Corporation
Medical Device
FDA DevicesClass I

Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

May 13, 2026AVID Medical, Inc.
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITH...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalo...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Medical Device
FDA DevicesClass I

VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000

Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could occur that may lead to reduced below intended levels of fraction of inspired oxygen delivery prior to and during ventilation and this oxygen-enriched environment may increase fire risk

May 13, 2026Ventec Life Systems, Inc.
Medical Device
FDA DevicesClass II

See RES for complete list. Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS, Mo...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

Medline Convenience Kits: 1) DYNDA3003, Model Number: DENTAL PACK; 2) DYNJ871...

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

May 13, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalo...

Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

May 13, 2026Katalyst Surgical, LLC
Medical Device
FDA DevicesClass I

Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G473...

Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

May 13, 2026Cook Incorporated
Medical Device
FDA DevicesClass I

Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx O...

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

May 13, 2026Medical Action Industries, Inc. 306
Food & Beverage
FDA FoodClass I

Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kra...

Product has the potential to be contaminated with Salmonella.

May 13, 2026Givaudan Flavors Corp
Medical Device
FDA DevicesClass I

Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G312...

Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.

May 13, 2026Cook Incorporated
sans marque - reblochon fermier aop
RappelConsovolontaire (san...

sans marque - reblochon fermier aop

présence de escherichia coli stec

May 13, 2026sans marque
le farto de thones - reblochon fermier aop
RappelConsovolontaire (san...

le farto de thones - reblochon fermier aop

présence de escherichia coli stec

May 13, 2026le farto de thones
sans marque - fromage montagnard
RappelConsovolontaire (san...

sans marque - fromage montagnard

présence de escherichia coli stec

May 13, 2026sans marque
← PreviousPage 104 of 3,016Next →