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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline epidural tray recalled for Lidocaine quality issues
Medline's L&D Continuous Epidural Tray (Model PAIN1699A) contains Lidocaine Ampules that were recalled by the manufacturer, Huons Co., Ltd., due to quality problems found during an FDA inspection. About 432 kits with this component have been distributed nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline Lumbar Puncture Kit recalled for Lidocaine quality issues
Medline's Lumbar Puncture Choice Kit (Model DYNDH1215) contains Lidocaine Ampules manufactured by Huons Co., Ltd. that have quality issues identified during an FDA inspection of the manufacturer's facility. The affected kits were distributed nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline medical kits recalled for Lidocaine quality issues
Medline Industries is recalling two medical convenience kits that contain Lidocaine Ampules from Huons Co., Ltd. The Lidocaine was flagged for quality issues during an FDA inspection of the manufacturer's facility. About 250 kits were distributed nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline convenience kits recalled for lidocaine quality issues
Multiple Medline medical kits containing lidocaine ampules manufactured by Huons Co., Ltd. are being recalled due to quality issues found during an FDA inspection of Huons' manufacturing facility. The affected kits are used for various surgical and medical procedures including suturing, chest tube insertion, biopsies, and arterial line placement.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline procedure kits recalled for defective lidocaine
Medline Industries has recalled multiple medical procedure kits (central line, arterial line, dialysis, biopsy, and suturing kits) because they contain lidocaine ampules with quality issues. The lidocaine supplier, Huons Co., Ltd., issued a recall after the FDA inspected their manufacturing site and identified problems. No injuries have been reported.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline suturing kits recalled for Lidocaine quality issues
Medline Convenience Kits (Model SUT13710) contain Lidocaine Ampules that were subject to a recall by the manufacturer Huons Co., Ltd. due to quality issues found during an FDA inspection of their manufacturing facility. About 176 kits were distributed nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline biopsy kits recalled for lidocaine quality issues
Medline's Imaging Biopsy Tray (Model DYNDH1068) and Breast Biopsy Pack (Model PHS234706I) contain lidocaine ampules that were identified as defective during an FDA manufacturing inspection. The ampules were supplied by Huons Co., Ltd. and may not meet quality standards. Approximately 40 kits are affected nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits recalled for lidocaine quality issues
Medline Convenience Kits containing Huons Lidocaine HCL Injection ampules are being recalled due to quality issues found during an FDA manufacturing inspection. The affected kits include two introducer models (6F and 9F) distributed nationwide. No injuries have been reported.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits recalled for Lidocaine quality issues
Medline Industries is recalling three models of medical convenience kits that contain Lidocaine Ampules manufactured by Huons Co., Ltd. The ampules were recalled due to quality issues found during an FDA inspection of the manufacturing facility. The affected kits are used in radiology, pain management, and endovenous procedures.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline central line kits recalled for defective lidocaine
Medline is recalling 34 different models of central line insertion kits that contain lidocaine ampules manufactured by Huons Co., Ltd. The ampules were found to have quality issues during an FDA inspection of the manufacturer's facility. Approximately 967 kits are affected.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline Convenience Kits recalled for Lidocaine quality issues
Medline's Convenience Kits (Model DYNJRA1590) contain Lidocaine Ampules that were recalled by the manufacturer, Huons Co., Ltd., due to quality issues found during an FDA manufacturing inspection. About 270 kits were distributed nationwide.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline epidural kits recalled for lidocaine quality issues
Medline distributed convenience kits containing lidocaine ampules manufactured by Huons Co., Ltd. The FDA identified quality issues with the lidocaine during a manufacturing inspection of Huons' facility. The affected kits are used for epidural anesthesia and pain management procedures.
- 2026-07-08FDA-DeviceMedline Industries, LPClass IIMedline arterial kits recalled for Lidocaine quality issues
Medline's arterial access and line insertion kits contain Lidocaine ampules from Huons Co., Ltd. that have quality defects. The defects were identified during an FDA inspection of the Lidocaine manufacturer's facility. The affected kits were distributed nationwide.
- 2026-07-08FDA-DeviceHamilton Medical AGClass IHamilton Medical ventilator breathing circuits recalled for valve obstruction risk
Certain coaxial breathing circuit sets used with Hamilton Medical ventilators (models C1, T1, and MR1) may have expiratory valve membranes that stick to the valve body. This defect is not always detectable before use and can trigger an "exhalation obstructed" alarm during ventilation, potentially leading to inadequate ventilation and oxygen desaturation in patients.
- 2026-07-08FDA-FoodNARA ORGANICS INCClass INara Organics infant formula recalled for botulism risk
Nara Organics Whole Milk Organic Infant Formula in two sizes may be contaminated with Clostridium botulinum, a bacterium that can cause botulism. The contamination was identified in specific lot codes with use-by dates between March 2027 and February 2028. No illnesses have been reported.
- 2026-07-08FDA-FoodFry Pie Factory LLCClass IIFry Pie Factory pepperoni rolls recalled for undeclared milk
Fry Pie Factory pepperoni rolls may contain milk that is not listed on the label. Additionally, some units were not kept refrigerated as required, which can allow harmful bacteria to grow. The recall affects 850 individually packaged 5 oz rolls with sell-by dates from June 12, 2026 through June 21, 2026, distributed in Ohio and West Virginia.
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIVista MAX dietary supplement recalled for undeclared Yellow#5
Vista MAX, a dietary supplement distributed by Vision of Health, contains Yellow#5 food dye that was not listed on the label. Yellow#5 can trigger allergic reactions in people sensitive to it. The affected product was distributed to local retail stores in California.
- 2026-07-08FDA-FoodProvision Health Corp. dba PH LabsClass IIProvision Health Ocular Plus recalled for undeclared Yellow#5
Ocular Plus, an eye health dietary supplement containing lutein and zeaxanthin, contains Yellow#5 food dye that was not listed on the label. Yellow#5 can trigger allergic reactions in sensitive individuals. About 7,000 units across three lot numbers were distributed to retail stores in California.
- 2026-07-08FDA-FoodMARS SNACKINGClass IIMorningStar Farms sausage patties recalled for plastic contamination risk
MorningStar Farms Hot & Spicy Sausage Patties (8 oz. bags, UPC 028989100948) may contain plastic material. The affected products have "Best If Used By" dates of July 5, 6, or 7, 2027 and were distributed nationwide.
- 2026-07-08FDA-FoodMARS SNACKINGClass IIMorningStar Farms vegan nuggets recalled for plastic contamination risk
MorningStar Farms Buffalo Chik'n Nuggets (10.5 oz bags, UPC 028989101105) may contain plastic material. The affected products have a "Best If Used By" date of July 7 or 8, 2027. No injuries have been reported.
- 2026-07-08FDA-FoodMOGO Moringa LLCClass IMOGO Pure Moringa capsules recalled for Salmonella risk
MOGO Pure Moringa Oleifera capsules may be contaminated with Salmonella Typhimurium. The contamination was discovered during testing. Affected bottles were sold online through Amazon, eBay, Etsy, and mogomiranga.com.
- 2026-07-08FDA-FoodWestern Mixers Produce & Nuts, Inc.Class IFIRST STREET Dark Chocolate Raisins recalled for undeclared peanuts
FIRST STREET Dark Chocolate Raisins (9 oz packages) contain undeclared peanuts that are not listed on the label. The product was distributed to California retail stores. People with peanut allergies who consume this product could have a serious allergic reaction.
- 2026-07-08FDA-DrugCipla USA, Inc.Class IICipla Cinacalcet tablets recalled for N-nitroso impurity
Cipla USA is recalling Cinacalcet Hydrochloride 90 mg tablets (lot 5PB0563, expiring 4/30/2027) because they contain elevated levels of N-nitroso-cinacalcet, a potentially harmful impurity that exceeds acceptable daily intake limits. This is a manufacturing quality issue.
- 2026-07-08FDA-DrugCipla USA, Inc.Class IICipla Cinacalcet tablets recalled for N-nitroso impurity
Cipla USA is recalling certain batches of Cinacalcet Hydrochloride 60 mg tablets because they contain N-nitroso-cinacalcet, a chemical impurity, at levels above the FDA's acceptable daily intake. The affected lots were distributed nationwide. No injuries have been reported.
- 2026-07-08FDA-DrugCipla USA, Inc.Class IICipla Cinacalcet tablets recalled for impurity risk
Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 30 mg tablets because they contain elevated levels of N-nitroso-cinacalcet, a manufacturing impurity that exceeds FDA safety limits. The affected bottles were distributed nationwide.
- 2026-07-08FDA-DrugLannett Company Inc.Class IILannett amphetamine capsules recalled for labeling mix-up
Lannett Company distributed amphetamine extended-release capsules that contained only immediate-release pellets but were labeled as extended-release. This labeling error could result in incorrect dosing and medication timing for patients who depend on the extended-release formulation.
- 2026-07-08FDA-DrugAsclemed USA Inc.Class IIAsclemed Lidocaine HCl Injection recalled for sterility concerns
Asclemed USA Inc. is recalling Lidocaine HCl Injection USP 1% in 5 mL single-dose ampules due to lack of assurance of sterility. The affected lots were distributed nationwide. This is a precautionary measure to prevent potential infection risk from non-sterile product.
- 2026-07-08FDA-DrugAsclemed USA Inc.Class IIAccucaine lidocaine injection recalled for sterility concerns
Asclemed USA Inc. is recalling specific lots of Accucaine, a lidocaine injection used for local anesthesia, because the manufacturer cannot guarantee the product is sterile. This affects multiple lot numbers distributed nationwide.
- 2026-07-08FDA-DrugBoehringer Ingelheim Pharmaceuticals, Inc.Class IISynjardy XR tablets recalled for manufacturing deviation
Boehringer Ingelheim Pharmaceuticals is recalling one lot of Synjardy XR 12.5/1000 mg tablets due to manufacturing quality control issues. During production, an incorrect cleaning agent was used on equipment, and required testing of that equipment was not completed before the tablets were made.
- 2026-07-08FDA-DrugACCORD HEALTHCARE, INC.Class IIAccord levothyroxine tablets recalled for subpotency
Accord Healthcare is recalling one lot of levothyroxine sodium 300 mcg tablets because they may contain less active ingredient than labeled. This means the medication may not work as intended for patients who need it to manage thyroid conditions.