Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
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.
Food & BeverageFranceRappelConso

pinabel - pain de mie graines magiques lin, courge et chia

pinabel
RappelConsovolontaire (san...

pinabel - pain de mie graines magiques lin, courge et chia

teneur en acide cyanhydrique supérieure à la réglementation

Jul 15, 2026pinabel
Food & BeverageFranceRappelConso

pinabel - protein mie

pinabel
RappelConsovolontaire (san...

pinabel - protein mie

teneur en acide cyanhydrique supérieure à la réglementation

Jul 15, 2026pinabel
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.
Safety AlertAustraliaAustralia Products

Galmet ColdGal Brushable Paint

Unknown Firm
Galmet ColdGal Brushable Paint
Australia ProductsGarden tools an...

Galmet ColdGal Brushable Paint

The container may bulge or swell due to internal pressure build up. Contents can be expelled when the container is opened.

Jul 15, 2026
Food & BeverageFranceRappelConso

westmark - ecumoire »gallant«

westmark
RappelConsovolontaire (san...

westmark - ecumoire »gallant«

présence d'une amine aromatique primaire dépassant, le seuil réglementaire

Jul 15, 2026westmark
Food & BeverageFranceRappelConso

baraenn - pain de mie graines bénéfiques chia, lin brun, courges

baraenn
RappelConsovolontaire (san...

baraenn - pain de mie graines bénéfiques chia, lin brun, courges

teneur en acide cyanhydrique supérieure à la réglementation

Jul 15, 2026baraenn
PharmaceuticalUSFDA Drugs

Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR 00924, UPC 659685696567.

Gasco Industrial Corp.
FDA DrugsClass II

Drogueria San Juan Puerto Rico Isopropyl Alcohol 70%, 32 oz., 946 mL, Distributed by: Drogueria San Juan, Calle De Diego 590, Sabana Llana Rio Piedras, PR 00924, UPC 659685696567.

Subpotent drug

Jul 15, 2026Gasco Industrial Corp.
Safety AlertAustraliaAustralia Products

Trione in-desk power hub

Unknown Firm
Trione in-desk power hub
Australia ProductsPower supply an...

Trione in-desk power hub

Due to an internal fault the power hub can overheat, burn and melt.

Jul 15, 2026
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
PharmaceuticalUSFDA Drugs

Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.

Gasco Industrial Corp.
FDA DrugsClass II

Gasco Isopropyl Alcohol 70%, 32 oz (946 mL) Gasco Industrial Corp., PO Box 1360, Gurabo PR 00778, UPC 7 87302 12363 6.

Subpotent drug

Jul 15, 2026Gasco Industrial Corp.
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

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

Elekta, Inc.
FDA DevicesClass II

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

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

TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components

Think Surgical, Inc.
FDA DevicesClass II

TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components

Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.

Jul 15, 2026Think Surgical, Inc.
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

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
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

sans marque - poitrine de porc indienne

sans marque
RappelConsovolontaire (san...

sans marque - poitrine de porc indienne

salmonelle

Jul 15, 2026sans marque
Medical DeviceUSFDA Devices

Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C

Medline Industries, LP
FDA DevicesClass II

Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C

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
Food & BeverageUSFDA Food

Johnny's Salad and Pasta Elegance 5.5 oz (UPC: 0-70381-10014-9) " Johnny's Salad and Pasta Elegance 2.75 oz (UPC: 0-70381-10013-2)

Adams Extract & Spice LLC
FDA FoodClass II

Johnny's Salad and Pasta Elegance 5.5 oz (UPC: 0-70381-10014-9) " Johnny's Salad and Pasta Elegance 2.75 oz (UPC: 0-70381-10013-2)

Undeclared Sesame allergen

Jul 15, 2026Adams Extract & Spice LLC
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

Nissan North America, Inc. - Incorrect GAWR on Certification Label/FMVSS 110

Nissan North America, Inc.
NHTSAEQUIPMENT

Nissan North America, Inc. - Incorrect GAWR on Certification Label/FMVSS 110

An overloaded vehicle can increase the risk of a crash.

Jul 15, 2026Nissan North America, Inc.
Food & BeverageFranceRappelConso

konouz - m.n.s - sesame dore

konouz - m.n.s
RappelConsovolontaire (san...

konouz - m.n.s - sesame dore

presence de chlorpyrifos

Jul 15, 2026konouz - m.n.s
Food & BeverageUSFDA Food

Smoked Sausage Spice 32.86#

Adams Extract & Spice LLC
FDA FoodClass I

Smoked Sausage Spice 32.86#

Undeclared Sesame allergen

Jul 15, 2026Adams Extract & Spice LLC

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