Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
Medical DeviceUSFDA Devices

VITEK 2 AST-N447 TEST KIT Product reference 424620

Biomerieux Inc
FDA DevicesClass II

VITEK 2 AST-N447 TEST KIT Product reference 424620

Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.

Jul 15, 2026Biomerieux Inc
Food & BeverageFranceRappelConso

declic garden - rateau enfant bois 61.5x18x7.5cm

declic garden
RappelConsovolontaire (san...

declic garden - rateau enfant bois 61.5x18x7.5cm

dents saillantes du râteau provoquant un risque de blessure

Jul 15, 2026declic garden
Food & BeverageFranceRappelConso

cpnp - saumon cuit nature

cpnp
RappelConsovolontaire (san...

cpnp - saumon cuit nature

erreur de cuisson : saumon encore cru à coeur

Jul 15, 2026cpnp
Vehicle RecallUSNHTSA

Orange EV - Frame Rails May Crack

Orange EV
NHTSASTRUCTURE

Orange EV - Frame Rails May Crack

A detached rail can cause a loss of control, increasing the risk of injury.

Jul 15, 2026Orange EV
Medical DeviceUSFDA Devices

5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing Set; Model Number: 03-5300-3. 4. 5008X HD/HDF With CLiC Blood Tubing Set; Model Number: 03-5300-3C. 5. 5008X HD/HDF With Twister Blood Tubing Set; Model Number: 03-5350-8.

Fresenius Medical Care Holdings, Inc.
FDA DevicesClass II

5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing Set; Model Number: 03-5300-3. 4. 5008X HD/HDF With CLiC Blood Tubing Set; Model Number: 03-5300-3C. 5. 5008X HD/HDF With Twister Blood Tubing Set; Model Number: 03-5350-8.

Potential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the 5008X CAREsystem.

Jul 15, 2026Fresenius Medical Care Holdings, Inc.
Medical DeviceUSFDA Devices

Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.

Elekta, Inc.
FDA DevicesClass II

Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Jul 15, 2026Elekta, Inc.
Medical DeviceUSFDA Devices

Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A

Medline Industries, LP
FDA DevicesClass II

Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

Jul 15, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.

Siemens Healthcare Diagnostics, Inc.
FDA DevicesClass II

Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536.

The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patient results.

Jul 15, 2026Siemens Healthcare Diagnostics, Inc.
Medical DeviceUSFDA Devices

Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.

Elekta, Inc.
FDA DevicesClass II

Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed for interstitial brachytherapy.

Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.

Jul 15, 2026Elekta, Inc.
Medical DeviceUSFDA Devices

Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/rigid

Olympus Corporation of the Americas
FDA DevicesClass II

Olympus Single Use Distal Cover, Catalog Number MAJ-2315, Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to be attached to Olympus duodenovideoscopes to cover the distal end of the insertion tube and around the forceps elevator; duodenoscope and accessories, flexible/rigid

Olympus has developed and released newly designed version of the Distal Cover (MAJ-2315) to replace previous design of the Single Use Distal Covers.

Jul 15, 2026Olympus Corporation of the Americas
Medical DeviceUSFDA Devices

Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed for surgeons to perform minimally invasive surgery.

CMR SURGICAL LIMITED
FDA DevicesClass II

Brand Name: Versius Surgical System US Product Name: Vesius Surgeon Console US Model/Catalog Number: V-SS-1020 Software Version: Pratchett 1 version 62.1 Product Description: The Versius Surgical System is a modular, open console, software controlled, electromechanical system designed for surgeons to perform minimally invasive surgery.

Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk.

Jul 15, 2026CMR SURGICAL LIMITED
Medical DeviceUSFDA Devices

Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R

ConvaTec, Inc
FDA DevicesClass II

Aquacel Ag Surgical SP REF: 413556 9cm x 15cm/3.5 in. x 6 in., Sterile R

Surgical dressing manufactured out of specification (greater thickness).

Jul 15, 2026ConvaTec, Inc
Medical DeviceUSFDA Devices

GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.

WALLAC OY
FDA DevicesClass II

GSP Neonatal GALT Kit. Product Codes: 3303-001U, 3303-0010. in vitro diagnostic. Used in FLUORESCENT PROC. (QUAL), GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.

Reduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting of patient results.

Jul 15, 2026WALLAC OY
Food & BeverageFranceRappelConso

fait maison - céleri remoulade

fait maison
RappelConsovolontaire (san...

fait maison - céleri remoulade

présence de corps étrangers

Jul 15, 2026fait maison
Medical DeviceUSFDA Devices

KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,

Klowen Braces
FDA DevicesClass II

KL Owen Custom Orthodontic Solution, model/catalog number CIAS-800033,

A product error defect may cause incorrect bracket placement.

Jul 15, 2026Klowen Braces
Vehicle RecallUSNHTSA

Hyundai Motor America - Seat Belt Buckle May Fail

Hyundai Motor America
NHTSASEAT BELTS

Hyundai Motor America - Seat Belt Buckle May Fail

A seat belt buckle that fails to properly restrain an occupant in a crash increases the risk of injury.

Jul 14, 2026Hyundai Motor America
Medical DeviceUKUK

Field Safety Notices: 6 to 10 July 2026

MHRAUK
uk-mhraMedical Device ...

Field Safety Notices: 6 to 10 July 2026

List of Field Safety Notices from 6 to 10 July 2026....

Jul 14, 2026MHRA
Vehicle RecallUSNHTSA

Wabash National Corporation - Liftgate Deck Pins May Break

Wabash National Corporation
NHTSASTRUCTURE

Wabash National Corporation - Liftgate Deck Pins May Break

A liftgate that falls unexpectedly increases the risk of injury.

Jul 14, 2026Wabash National Corporation
Food & BeverageGermanyGermany BVL

Labneh Al Raii Original Bucket

Hersteller: Al Raii Inverkehrbringer: Alshalati, Großhandel für orientalische Lebensmittel, August-Wilhelm Kühnholz Straße 8 26135 Oldenburg
Germany BVLGeneral Alert

Labneh Al Raii Original Bucket

Sonstige Gründe

Jul 14, 2026Hersteller: Al Raii Inverkehrbringer: Alshalati, Großhandel für orientalische Lebensmittel, August-Wilhelm Kühnholz Straße 8 26135 Oldenburg
Food & BeverageUKUK FSA

Lidl Northern Ireland recalls 1001 Delights Dubai Style Pistachio Ice Cream because of undeclared cashew (nuts)

Lidl Northern Ireland
UK FSAPublished

Lidl Northern Ireland recalls 1001 Delights Dubai Style Pistachio Ice Cream because of undeclared cashew (nuts)

This product contains cashew (nuts) making it a possible health risk for anyone with an allergy to cashews.

Jul 14, 2026Lidl Northern Ireland
Food & BeverageFranceRappelConso

brassée 24 - ginger beer

brassée 24
RappelConsovolontaire (san...

brassée 24 - ginger beer

surpression dans les bouteilles

Jul 14, 2026brassée 24
Food & BeverageFranceRappelConso

fût sarladais - ginger beer

fût sarladais
RappelConsovolontaire (san...

fût sarladais - ginger beer

surpression dans les bouteilles

Jul 14, 2026fût sarladais
Vehicle RecallUSNHTSA

Winnebago Industries, Inc. - Printed Circuit Board May Overheat

Winnebago Industries, Inc.
NHTSAGeneral Alert

Winnebago Industries, Inc. - Printed Circuit Board May Overheat

An overheated printed circuit board increases the risk of a fire.

Jul 14, 2026Winnebago Industries, Inc.
Safety AlertAustraliaAustralia Products

Toe warmers 2pk

Unknown Firm
Toe warmers 2pk
Australia ProductsHeating and coo...

Toe warmers 2pk

When the product is used, it may inflate and heat rapidly. The product can become very hot and burst open.

Jul 14, 2026

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.