Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,116 results
Safety AlertUSCPSC

Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard

Unknown Firm
Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard
CPSCGeneral Alert

Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard

The recalled chairs' base can bend, posing a fall hazard.

Mar 19, 2026
Medical DeviceUSFDA Devices

EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;

Boston Scientific Corporation
FDA DevicesClass II

EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;

Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of sterility or drying of the antiseptic solution. This component is placed outside of the sterile barrier of the tray manufactured by Boston Scientific, which contains the majority of the kit components. As such, inclusion of the affected ChloraPrep Triple Swabsticks does not degrade the integrity of the other components within the PEG kit.

Mar 18, 2026Boston Scientific Corporation
Medical DeviceUSFDA Devices

Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X

Penner Patient Care, Inc.
FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X

The device does not bear a unique device identifier.

Mar 18, 2026Penner Patient Care, Inc.
Medical DeviceUSFDA Devices

Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,L MDTGXP4JXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTGXP4JXXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XX MDTL1002862EF DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTZ1000893AJ DBD-GOWN,SRG,PNL CVR, GREEN,SNPS,XL

Medline Industries, LP
FDA DevicesClass II

Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,L MDTGXP4JXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTGXP4JXXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XX MDTL1002862EF DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTZ1000893AJ DBD-GOWN,SRG,PNL CVR, GREEN,SNPS,XL

Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.

Mar 18, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

Penner Patient Care, Inc.
FDA DevicesClass III

Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

The device does not bear a unique device identifier.

Mar 18, 2026Penner Patient Care, Inc.
Medical DeviceUSFDA Devices

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

Becton Dickinson & Company
FDA DevicesClass II

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

Mar 18, 2026Becton Dickinson & Company
Vehicle RecallUSNHTSA

Jaguar Land Rover North America, LLC - Insufficiently Welded Seat Belt Anchorage Bracket

Jaguar Land Rover North America, LLC
NHTSASEAT BELTS

Jaguar Land Rover North America, LLC - Insufficiently Welded Seat Belt Anchorage Bracket

A seat belt assembly with an insufficient weld may not properly restrain an occupant during a crash, increasing the risk of injury.

Mar 18, 2026Jaguar Land Rover North America, LLC
Medical DeviceUSFDA Devices

GEM Premier 5000; Part No. 00055445010 & 00055445011.

Instrumentation Laboratory
FDA DevicesClass II

GEM Premier 5000; Part No. 00055445010 & 00055445011.

Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.

Mar 18, 2026Instrumentation Laboratory
Food & BeverageFranceRappelConso

acevia - porchetta coussin 1/2

acevia
RappelConsovolontaire (san...

acevia - porchetta coussin 1/2

présence de listeria monocytogenes

Mar 18, 2026acevia
Food & BeverageFranceRappelConso

laleu - magret de canard séché tranché au poivre

laleu
RappelConsovolontaire (san...

laleu - magret de canard séché tranché au poivre

non conformité microbiologique

Mar 18, 2026laleu
Food & BeverageFranceRappelConso

primark - gourde cinnamoroll - 500ml

primark
RappelConsovolontaire (san...

primark - gourde cinnamoroll - 500ml

ce produit ne satisfait pas aux exigences de la norme en 14350

Mar 18, 2026primark
Medical DeviceUSFDA Devices

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Medartis AG
FDA DevicesClass II

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.

Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

Mar 18, 2026Medartis AG
Food & BeverageFranceRappelConso

- - masques de carnaval

-
RappelConsovolontaire (san...

- - masques de carnaval

un contrôle a mis en évidence l’absence de mise en relief de l’allergène lait dans la liste d’ingrédients du produit.

Mar 18, 2026-
Food & BeverageFranceRappelConso

metro chef - bloc serrano 2.2kg env metro chef

metro chef
RappelConsovolontaire (san...

metro chef - bloc serrano 2.2kg env metro chef

présence de listeria monocytogènes

Mar 18, 2026metro chef
Food & BeverageFranceRappelConso

saint alby - blanc de poulet

saint alby
RappelConsovolontaire (san...

saint alby - blanc de poulet

une analyse a mis en évidence la détection de salmonelle.

Mar 18, 2026saint alby
Food & BeverageFranceRappelConso

disney - fleurs de douche simba -gencod 3666085407553 -tous les lots

disney
RappelConsovolontaire (san...

disney - fleurs de douche simba -gencod 3666085407553 -tous les lots

présence de phtalates dans le badge décoratif amovible associé à la fleur de douche - personnage simba. ces composés ont des effets négatifs sur la santé.

Mar 18, 2026disney
Food & BeverageFranceRappelConso

u - lomo espagnol 20 tranches u 100g

u
RappelConsovolontaire (san...

u - lomo espagnol 20 tranches u 100g

non conformite microbiologique

Mar 18, 2026u
Food & BeverageFranceRappelConso

travel folding electeic kettle bouilloire électrique

Unknown Firm
RappelConsoGeneral Alert

travel folding electeic kettle bouilloire électrique

le produit n'a pas une résistance mécanique suffisante et pourrait donc facilement se casser en cas d'impact ou de chute du produit. de plus, les connecteurs des fils alimentant l'interrupteur bimétallique et l'élément chauffant ne sont pas correctement sertis et pourraient se détacher avec le temps. le produit a également des distances de dégagement insuffisantes. tout cela pourrait rendre les pièces sous tension accessibles à l'utilisateur, qui pourrait recevoir un choc électrique. de plus, la prise électrique n'est pas conforme, ce qui pourrait entraîner une connexion lâche et une surchauffe du produit.

Mar 18, 2026
Food & BeverageFranceRappelConso

sans marque - gorgonzola dop à la cuillère

sans marque
RappelConsovolontaire (san...

sans marque - gorgonzola dop à la cuillère

présence de listeria monocytogenes.

Mar 18, 2026sans marque
Food & BeverageFranceRappelConso

veed - mondo gummies cbd

veed
RappelConsovolontaire (san...

veed - mondo gummies cbd

recommandation de consommation journalière conduisant a un dépassement de la dose de référence aiguë en delta 9 thc

Mar 18, 2026veed
Food & BeverageFranceRappelConso

vrac - cookie 30mg cbd

vrac
RappelConsovolontaire (san...

vrac - cookie 30mg cbd

recommandation de consommation journalière conduisant a un dépassement de la dose de référence aiguë en delta 9 thc

Mar 18, 2026vrac
Food & BeverageFranceRappelConso

vibes - cookie 150mg cbd

vibes
RappelConsovolontaire (san...

vibes - cookie 150mg cbd

recommandation de consommation journalière conduisant a un dépassement de la dose de référence aiguë en delta 9 thc

Mar 18, 2026vibes
Food & BeverageFranceRappelConso

acevia - fromage de tête

acevia
RappelConsovolontaire (san...

acevia - fromage de tête

présence de listeria monocytogenes

Mar 18, 2026acevia
Medical DeviceUSFDA Devices

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Exactech, Inc.
FDA DevicesClass II

Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle Model/Catalog Number: 321-09-05

Impactor handle may be missing cross-pin

Mar 18, 2026Exactech, Inc.

Install The Recall File App

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