68 recalls tagged with “plastic”.
Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.
More than 1.02 million bottles of Dry Eye Relief Eye Drops across multiple brands were recalled nationwide on March 3, 2026. The products were distributed by KC Pharmaceuticals and sold at retailers including Rite Aid, Meijer and H-E-B. The FDA notice cites a lack of assurance of sterility as the reason for the recall. Stop using these products immediately and contact KC Pharmaceuticals for next‑s
Ajinomoto Foods North America recalled Trader Joe's Vegetable Fried Rice sold at Trader Joe's nationwide after glass fragments were found in the product. The contamination involves glass shards ranging from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should contact Ajinomoto Foods North America for refunds or replacements.
Quality Choice Moisturizing Relief Eye Drops and Foster & Thrive Advanced Relief Eye Drops are recalled after 303,216 bottles distributed nationwide through Walgreens, CVS and other retailers lack sterility. The defect is lack of assurance of sterility. Consumers should stop using the products immediately and contact KC Pharmaceuticals for guidance.
K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider
Civco Medical Instruments Co. recalled 21 eTRAX Needle Sensors for Aurora Trackers sold to healthcare providers in Ohio, Pennsylvania and Washington. The devices have an inspection and programming error that can cause the needle tip position to be misidentified on the user interface. Clinicians should stop using the devices immediately and follow recall instructions from Civco.
Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.
4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.
Olympus Corporation of the Americas recalled 93 PKS Cutting Forceps worldwide due to welding defects that can cause the jaw to break during clinical use. The issue involves Model 3005PK and UDI 00821925036000. Action is required immediately and providers should follow recall instructions.
Pacific Coast Fresh Co. recalled 760 King Harvest Jalapeno Hummus containers distributed in Oregon and Washington. Aluminum pieces were found as a foreign material in the product. Consumers should not consume this hummus and should contact the company for refund or replacement.
King Harvest Balsamic Hummus recalled by Pacific Coast Fresh Co. The product was distributed in Oregon and Washington. A foreign material aluminum piece hazard was identified. Consumers should not eat the product and should contact Pacific Coast Fresh Co for refund or replacement information by telephone.
Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.
Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-
Medline Industries recalled 420 Sterile Radiology Procedure Kits, Model DYNDH1491B, distributed nationwide in Minnesota after a potential breach in sterile pouch packaging. The defect may compromise product sterility. Stop using the kit immediately and contact Medline or your healthcare provider for instructions.
Medline Industries, LP recalled 14,379 kits nationwide that include Olympus biopsy valves. The recall concerns rubber fragments detaching in the slit of single-use biopsy valves. Stop using these kits immediately and follow manufacturer instructions for return or replacement.
Olympus Corporation of the Americas is recalling 2,929 units of the OER-Elite Endoscope Reprocessor in the United States. The MAJ-1443 and MAJ-1444 modules are no longer reprocessing compatible with the OER-Pro and OER-Elite systems. Hospitals and healthcare providers should stop using the affected devices immediately and follow the recall instructions issued by Olympus.
Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.
Burlington Medical recalled 402 Half Aprons sold worldwide after potential attenuation degradation. Attenuation material Xenolite 800 may degrade over time, reducing shielding lifespan. Patients and healthcare providers should stop using the aprons immediately and contact Burlington Medical for recall instructions.
Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.
Burlington Medical recalled 5,198 wrap aprons worldwide after attenuation degradation was identified in Xenolite 800 material. The recall covers units manufactured between 01/16/2025 and 01/21/2026. Stop using the aprons immediately and follow the manufacturer’s recall instructions.