Safety Recall Directory

HardyDisk AST Cefiderocol 30¿g (FDC30) REF Z9435 HardyDisk AST Cefiderocol 30¿g (FDC30) for in vitro agar diffusion susceptibility testing is indicated when there is the need to determine the susceptibility of Enterobacterales, Pseudomonas aeruginosa, Acinetobacter baumannii complex and Stenotrophomonas maltophilia to Cefiderocol,

Due to incorrect cartridges include in affected products that there is the potential for false-susceptible or false-resistant susceptibility results and may lead to selection of an ineffective antimicrobial therapy, potentially resulting in delayed appropriate treatment, prolonged infection, or worsening clinical outcome.

Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475625 Product Description: Intramedullary Bone Saw Blade Assembly 13mm

Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.

5-PLASMA Bivalirudin Control, Model Number 5D-44905

Stability issues with the reconstituted lyophilized human plasma and bivalirudin matrix have been identified. These stability issues lead to a degradation of measurable bivalirudin in the controls, calibrators, and linearity values.

the glowhouse - flashing princess wand

accessibilité des piles boutons consécutive à la présence d'une vis perdable. risque d'ingestion, de brûlure ou d'intoxication.

Flexible food pouch (3-layer foil, spouted, #CP6088), manufactured for packaging Pumpkin Tree Peter Rabbit Organics Banana & Strawberry, 4 oz food puree, UPC 815367010780.

Flexible food pouch may release thin plastic strips into food.

Philips Azurion under the following System Descriptions and corresponding model numbers: 1. Azurion 3 M12; Model Numbers: 722063, 722221. 2. Azurion 3 M15; Model Numbers: 722064, 722222, 722280. 3. Azurion 5 M12; Model Number: 722227. 4. Azurion 5 M20; Model Numbers: 722228, 722281. 5. Azurion 7 B12; Model Numbers: 722067, 722225. 6. Azurion 7 B20; Model Numbers: 722068, 722226. 7. Azurion 7 M12; Model Numbers: 722078, 722223. 8. Azurion 7 M20; Model Numbers: 722079, 722224, 722282. Interventional Fluoroscopic X-Ray System.

Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.

Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530 Flow-i C40 6888540 Flow-c 6887700 Flow-e 6887900

Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient receiving insufficient anesthesia and may lead to intraoperative awareness.

sans marque - crevettes roses cuites étal poissonnerie

présence listéria monocytogènes

sans marque - langoustines glacées 20/40

taux de sulfites dépassant le seuil réglementaire

tous type de marque - glaces

rupture de la chaîne du froid

Field Safety Notices: 3 to 7 August 2026

List of Field Safety Notices from 3 to 7 August 2026....

carrefour sensation - dipster saveur crème oignon

mise en évidence d’un rancissement précoce en raison d’une oxydation de l’huile de friture.

Frankie's Organic Issues Allergy Alert on Undeclared Milk in Frankie’s Organic Plant-Based Vegan Cheddar Puffs

signature du poissonnier - crevettes entières cuites réfrigérées élevage 40/60 mada 300g et sauvage fao 51.6 320g

présence listéria monocytogènes

Henkel Corp. Announces a Nationwide Recall of Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml Due to Packaging Imperfection

Lidl US Recalls Vitasia Asian Style Wok Spice Mix Due to Potential Salmonella Contamination

Recall of Jalapeno Avocado Dressing Because of Possible Health Risk

Devices supplied without valid UKCA/CE conformity markings or certification: remove from use and place in quarantine (DSI/2026/007)

The MHRA has become aware of a number of medical devices being supplied on the UK market that do not comply with the requirements of the UK Medical Device Regulations 2002 (UK MDR 2002) or with the EU...

smilekit - stylo pour le blanchiment dentaire - smile kit

le produit contient 7,6% de peroxyde d'hydrogène, dépassant la limite réglementaire stricte de 0,1% pour les produits grand public, ce qui présente un risque grave de brûlures ou lésions des muqueuses et de la peau.

sans marque - viande hachee

détection de listéria monocytogènese <10 ufc/g

sans marque - produits élaborés saurisserie

un contrôle microbiologique a mis en évidence dans ce produit la présence de salmonelles

lamborghini - lamborghini huracan performante spyder

risques de lésions auditives (son de 90 db au lieu de 80 db max) et d'ingestion de piles (vis non imperdable). non-conformités réglementaires.

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.

Blue Bird Body Company - Damaged Wiring May Disrupt Critical Safety Functions

An electrical short can cause a disruption to safety functions such as a loss of rear lighting or instrument panel warning lights, increasing the risk of a crash.