Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 74,115 results
Medical DeviceUSFDA Devices

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)

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

Jul 1, 2026SURGIFY MEDICAL OY
Medical DeviceUSFDA Devices

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAM PACK-LF DYNJ21574J JUDKINS PACK DYNJ51126

Medline Industries, LP
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIOGRAM PACK-LF DYNJ21574J JUDKINS PACK DYNJ51126

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

Jul 1, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines & accessories (simple, powered)

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

Jul 1, 2026SURGIFY MEDICAL OY
PharmaceuticalUSFDA Drugs

hydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/5 mL, 473 mL (1 Pint), Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623. NDC: 70954-912-10

ANI Pharmaceuticals, Inc.
FDA DrugsClass III

hydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/5 mL, 473 mL (1 Pint), Rx only, Distributed by: ANI Pharmaceuticals, Inc., Baudette, MN 56623. NDC: 70954-912-10

Presence of foreign substance

Jul 1, 2026ANI Pharmaceuticals, Inc.
Medical DeviceUSFDA Devices

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS PACK DYNJ905160J DYNJ905160K DYNJ905160M MINIMALLY INVASIVE PACK-LF DYNJ0843063K PERCUTANEOUS TRAY DYNJ80196 ROBOTIC PACK DYNJ908706 DYNJ908706B

Medline Industries, LP
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS PACK DYNJ905160J DYNJ905160K DYNJ905160M MINIMALLY INVASIVE PACK-LF DYNJ0843063K PERCUTANEOUS TRAY DYNJ80196 ROBOTIC PACK DYNJ908706 DYNJ908706B

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

Jul 1, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905159F DYNJ905159I DYNJ905159J DYNJ905159K NEURO CERVICAL PACK DYNJ0101287J DYNJ0101287K NEURO SPINE PACK DYNJ81612C POSTERIOR SPINE PACK-LF DYNJ0843339L DYNJ0843339M DYNJ0843339N SPINE PACK DYNJ30150F

Medline Industries, LP
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905159F DYNJ905159I DYNJ905159J DYNJ905159K NEURO CERVICAL PACK DYNJ0101287J DYNJ0101287K NEURO SPINE PACK DYNJ81612C POSTERIOR SPINE PACK-LF DYNJ0843339L DYNJ0843339M DYNJ0843339N SPINE PACK DYNJ30150F

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

Jul 1, 2026Medline Industries, LP
Food & BeverageUSFDA Food

Joy Peach Lassi 16 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Peach Lassi 16 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Medical DeviceUSFDA Devices

GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System

GE Medical Systems SCS
FDA DevicesClass II

GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System

GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client worklist and launches an interactive application (e.g. Volume Viewer), the application may open the previous patient's exam instead of the intended one. When this issue occurs, there is no system warning or error notification. If the error is not recognized, a clinical user could review, interpret, or report images for the wrong patient which could lead to misdiagnosis, incorrect clinical decisions, resulting in delayed or incorrect treatment.

Jul 1, 2026GE Medical Systems SCS
Medical DeviceUSFDA Devices

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. AAA DYNJ905651B ARTERIOGRAM TRAY 00-402001S AV SHUNT PACK-LF DYNJ0842516F BASIC IR PACK-LF PHS463660F CATH PROCEDURAL TRAY DYNJ43580C CONGENITAL ADD-ON KIT DYNDA2213A CUSTOM PROCEDURE KIT DYNJ65277A DEEP BRAIN STIMULATION PACK DYNJ0842793F HOSPITAL REGIONAL DE CONCEPCIO DYNJ67918 INTERVENTIONAL PACK DYNJ56666B INVASIVE LINE INSERTION DYNJ44123A JUDKINS PACK DYNJ51126B LARKIN CUSTOM NEURO TRAY PAIN1454 MAJOR PLUS PACK DYNJ905160I MINIMALLY INVASIVE PACK-LF DYNJ0843063J NEURO ANGIO PACK SJF-LF DYNJ37304F NON-VASCULAR PACK DYNJ56386B OR HYBRID-MRMC DYNJ907758 PACER PACK DYNJ40952 PAIN PACK DYNJ60715 PICC PHC DYNJ37484B ROBOTIC PACK DYNJ908706A THORACOTOMY PACK-LF DYNJ0101339J DYNJ69090 VENOUS PACK DYNJ56260B

Medline Industries, LP
FDA DevicesClass II

Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. AAA DYNJ905651B ARTERIOGRAM TRAY 00-402001S AV SHUNT PACK-LF DYNJ0842516F BASIC IR PACK-LF PHS463660F CATH PROCEDURAL TRAY DYNJ43580C CONGENITAL ADD-ON KIT DYNDA2213A CUSTOM PROCEDURE KIT DYNJ65277A DEEP BRAIN STIMULATION PACK DYNJ0842793F HOSPITAL REGIONAL DE CONCEPCIO DYNJ67918 INTERVENTIONAL PACK DYNJ56666B INVASIVE LINE INSERTION DYNJ44123A JUDKINS PACK DYNJ51126B LARKIN CUSTOM NEURO TRAY PAIN1454 MAJOR PLUS PACK DYNJ905160I MINIMALLY INVASIVE PACK-LF DYNJ0843063J NEURO ANGIO PACK SJF-LF DYNJ37304F NON-VASCULAR PACK DYNJ56386B OR HYBRID-MRMC DYNJ907758 PACER PACK DYNJ40952 PAIN PACK DYNJ60715 PICC PHC DYNJ37484B ROBOTIC PACK DYNJ908706A THORACOTOMY PACK-LF DYNJ0101339J DYNJ69090 VENOUS PACK DYNJ56260B

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

Jul 1, 2026Medline Industries, LP
Food & BeverageUSFDA Food

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, 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).

Spring & Mulberry Inc.
FDA FoodClass I

Spring & Mulberry Mixed Berry Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470026, 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

Jul 1, 2026Spring & Mulberry Inc.
Safety AlertUSRSS Feed

Kao USA Voluntarily Recalls Some Lots of Oribe Serene Scalp Densifying Shampoo

Unknown Firm
RSS FeedGeneral Alert

Kao USA Voluntarily Recalls Some Lots of Oribe Serene Scalp Densifying Shampoo

Jul 1, 2026
Medical DeviceUSFDA Devices

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

Intuitive Surgical, Inc.
FDA DevicesClass II

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and may result in uncontrolled motion. In addition, if it moves/backs out it may cause restricted column range of motion and/or uncontrolled motion, which may cause patient tissue injury/crushing injury/bleeding.

Jul 1, 2026Intuitive Surgical, Inc.
Medical DeviceUSFDA Devices

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

IPG Medical Corporation
FDA DevicesClass II

Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.

Software anomaly that causes a false display of error code 5018.

Jul 1, 2026IPG Medical Corporation
Medical DeviceUSFDA Devices

Octopus Evolution Tissue Stabilizer, Model TS2000

Medtronic Perfusion Systems
FDA DevicesClass II

Octopus Evolution Tissue Stabilizer, Model TS2000

During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to the bottom of the canister, and the long tube was attached to the top, contrary to the intended design.

Jul 1, 2026Medtronic Perfusion Systems
Food & BeverageUSFDA Food

Joy Mango Lassi 16 oz., 64 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Mango Lassi 16 oz., 64 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Medical DeviceUSFDA Devices

INZONE DETACHMENT SYSTEM, REF: M00345100950

Stryker Neurovascular
FDA DevicesClass II

INZONE DETACHMENT SYSTEM, REF: M00345100950

Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual indicators; 3) Be unable to detach a coil as intended, which may necessitate medical intervention if the procedure must be completed with an alternative technique.

Jul 1, 2026Stryker Neurovascular
Medical DeviceUSFDA Devices

Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)

SURGIFY MEDICAL OY
FDA DevicesClass II

Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)

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

Jul 1, 2026SURGIFY MEDICAL OY
PharmaceuticalUSFDA Drugs

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner Carton, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-31.

CareFusion 213, LLC
FDA DrugsClass I

BD ChloraPrep Clear (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA)), 1 mL Applicator, 60 Applicators per inner Carton, Sterile Solution, Care Fusion 213, LLC, El Paso, TX 79912, subsidiary of Beckton, Dickinson and Co., NDC 54365-400-31.

Non-Sterility: Due to presence of Aspergillus penicillioides.

Jul 1, 2026CareFusion 213, LLC
Food & BeverageUSFDA Food

Joy Mango-Pina-Orange Lassi 16 oz., 64 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Mango-Pina-Orange Lassi 16 oz., 64 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Food & BeverageUSFDA Food

1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plastic Bag.

Utz Quality Foods, LLC
FDA FoodClass I

1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plastic Bag.

Potential presence of Salmonella.

Jul 1, 2026Utz Quality Foods, LLC
Food & BeverageUSFDA Food

2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.

Utz Quality Foods, LLC
FDA FoodClass I

2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.

Potential presence of Salmonella.

Jul 1, 2026Utz Quality Foods, LLC
Food & BeverageUSFDA Food

Joy Saffron Cardamon Lassi 16 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Saffron Cardamon Lassi 16 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.
Food & BeverageUKUK FSA

O’Brien Fine Foods recalls ham products because of possible contamination with Listeria monocytogenes

O’Brien Fine Foods
UK FSAPublished

O’Brien Fine Foods recalls ham products because of possible contamination with Listeria monocytogenes

 The possible presence of Listeria monocytogenes in the products listed above. Symptoms caused by Listeria monocytogenes can be similar to flu and include high temperature, muscle ache or pain, chills, feeling or being sick and diarrhoea. However, in rare cases, the infection can be more severe, causing serious complications, such as meningitis. Some people are more vulnerable to listeria infections, including those over 65 years of age, pregnant women and their unborn babies, babies less than one month old and people with weakened immune systems.

Jul 1, 2026O’Brien Fine Foods
Food & BeverageUSFDA Food

Joy Plain Chaash Lassi 16 oz., 64 oz.

Joy Gourmet Foods LLC.
FDA FoodClass II

Joy Plain Chaash Lassi 16 oz., 64 oz.

Product not adequately pasteurized

Jul 1, 2026Joy Gourmet Foods LLC.

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