2,228 recalls tagged with “stop use immediately”.
Olympus recalls 408 SOLTIVE Premium Laser System units worldwide after a defect in the 24V power supply may render the system inoperable and cause smoke or a burning smell. The issue is contained within the internal console and would self-extinguish. Hospitals should stop using the device immediately and follow recall instructions.
GE Healthcare recalled 41 SIGNA Premier Whole-Body MRI systems sold worldwide. The devices may have ferrous fittings on the magnet rear instead of brass. If service is performed while the magnet is ramped, the magnetic field could attract the fittings and injure personnel. Hospitals should stop using the devices and follow the manufacturer's recall instructions.
TG Foods recalled 7,980 units of Divided Sunset Multi Collagen Peptides 8 oz stand-up pouches distributed nationwide. The recall notes the ingredient statement lists wild caught marine collagen and eggshell membrane collagen but does not declare EGG or the specific fish species. Consumers should not consume the product and should contact TG Foods for refund or replacement information.
Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.
Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.
Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.
Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.
Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek
Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.
Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.
Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.
Medline Industries, LP recalls 108 NAMIC Angiographic Rotating Adaptor Syringes sold worldwide, including the United States, PR and several international markets. The rotating adaptor may unwind during use, creating a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions.
Medline Industries, LP recalled 240 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers worldwide distribution including the US, Puerto Rico, and multiple international markets. The potential issue is the adaptor unwinding during use, risking a loose connection or disconnection with the manifold.
Medline Industries, LP recalls 2,154 medical convenience kits worldwide after post-market surveillance found a risk that the NAMIC Angiographic Rotating Adaptor may unwind. A loose connection or disconnection between the syringe and manifold could occur. Stop using immediately and follow manufacturer recall instructions.
Medline Industries, LP recalled 82 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers two Medline SKUs and spans worldwide distribution, including the US, Puerto Rico and several countries. The defect is a rotating adaptor that may unwind, causing loose connections or disconnections between syringe and manifold.
Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.
Medline Industries, LP recalled 149,439 NAMIC Angiographic Syringes worldwide, including the US and several international markets. The post-market signal shows a potential rotation adaptor unwinding during use, which can cause a loose or complete disconnect with the manifold. Health care providers and patients should stop using the devices and follow Medline's recall instructions.
Medline Industries recalled 2,630,369 NAMIC Angiographic Syringes worldwide after post-market surveillance found a potential risk that the syringe rotating adaptor could unwind during use, causing a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions. Contact Medline or a healthcare provider for guidance.
Medline Industries, LP recalls 20 kits worldwide after post-market surveillance found a risk the syringe rotating adaptor may unwind during use, causing a loose connection or full disconnection with the manifold. The recall affects three Medline SKUs and includes UDI details and lot numbers. Healthcare providers and patients should stop using the device immediately and follow Medline's recall plan
Medline Industries, LP recalls 966 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers kits labeled DELIVERY PACK with SKUs DYNJ42892F and DYNJ42892G distributed worldwide, including the US and PR. The defect is a rotating adaptor that may unwind, creating a loose connection or disconnection between syringe and manifold. Stop using the device and use