Safety Recall Directory

Jayco, Inc. - Grounding Connection Not Installed

The electrical system may overheat without a ground, increasing the risk of a fire. There is also an increased risk of injury from electrical shock.

Nissan North America, Inc. - Rear Seat Belts May Not Secure Child Seat/FMVSS 208

An improperly secured child restraint system may not restrain an occupant as intended, increasing the risk of injury during a crash.

Jayco, Inc. - Grounding Connection Not Installed

The electrical system may overheat without a ground, increasing the risk of a fire. There is also an increased risk of injury from electrical shock.

Kia America, Inc. - Park Outside: High Voltage Battery May Catch Fire

A fire increases the risk of injury.

Kia America, Inc. - Park Outside: Fire from Overheated Power Seat Motors

A fire increases the risk of injury.

prescription nature - creatine premium

cuillère doseuse non conforme au niveau de la quantité délivrée

Hyundai Motor America - Park Outside: High Voltage Battery May Catch Fire

A fire increases the risk of injury.

NephroMax High Pressure Nephrostomy Balloon Catheter

Device compatibility

Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fire Hazard

The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard.

Fludeoxyglucose (18F) Injection; Cracked vial

Product quality

grand frais / fresh - eminces de truite aneth 100g

détection listeria monocytogenes

New Horse Riding Helmet 100 Fouganza recalled due to injury hazard

Injury hazard

RAPIDLab® 348EX System

Performance

Glidesheath Slender® Introducer Sheath

Performance

WASPLab

Performance

hyundai - kona voiture particulière

le logiciel de surveillance de la batterie est défectueux et est incapable de détecter rapidement l'instabilité thermique dans la batterie haute tension conduisant à un incendie.

Gellert Global Group Issues Allergy Alert on Undeclared Tuna (Fish) in Aldi Brand Fusia Asian Inspirations Kimchi and Tofu Kimbap

LIFECODES LSA Class II

Performance

Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.U1; drills, burrs, trephines & accessories (simple, powered)

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).

carrefour bio - abricots moelleux carrefour bio 250 g dénoyautés

présence de sulfites, non mentionnée sur l’étiquetage

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO CATH COMBINED PACK DYNJ43609S ANGIO PACK DYNJ67987D DYNJ80317A ANGIO SPECIAL PROCEDURE-LF DYNJ38412C ANGIOGRAM SET UP PACK DYNJ66260A ANGIOGRAPHY PACK DYNJ44293I ANGIOGRAPHY PACK-LF DYNJ0854485W CARDIAC CATH PACK DYNJ82709 CARDIAC CATH PACK-LF DYNJ0261554AL DYNJ31103F CATH LAB ANGIO TRAY DYNJ83506 CATH LAB PACK DYNJ66366C MSC-GREEN BAY ST VINCENT SAMPC0686 NEUROLOGICAL CATH PACK DYNJ63434B OR HYBRID-MRMC DYNJ907758B STEWARD OR ANGIO PACK GSS DYNJ80925B

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.

Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470231, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag, (patient specific), Rx# 24-1269856-0-1Compound Volume 1295 mL per bag, Rx only, Single Dose Injection, Refrigerated Injection, Central Admixture Pharmacy Services, Boston, 55 6th Rd Woburn, Massachusetts 01801-1767.

Incorrect product formulation: bag did not contain copper and famotidine per label.

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR G'S BREAST PACK DYNJ51124B LIPO SUPPLEMENT PACK-LF DYNJ0341174D PLASTIC PACK DYNJ66746 DYNJ85702

Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601.