Recalls published in July 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in July 2026, newest first.
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Class II · 4 months ago
Carl Zeiss Meditec AG Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 recall: Spherical applicators (radiation therapy accessory) failed to meet
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
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Class II · 4 months ago
Medline Convenience kits containing recalled Swan-Ganz Catheters Open recall: Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue)…
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Class II · 4 months ago
Medline Convenience Kits: 1) Imaging Biopsy Tray recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class II · 4 months ago
Medline Convenience Kits: 1) STD, Intro-Flex Introducer 6F, C recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class II · 4 months ago
Bard Access Systems, Inc. 5855240 Power-Trialysis Slim-Cath Straight Short-Term recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Masimo Corporation Radius VSM ECG pre-connected Set, REF: 4842, 4695 recall: Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG
Two devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger…
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Class II · 4 months ago
Medline Convenience Kits: 1) Suture Tray recall: The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd…
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Class II · 4 months ago
Teleflex LLC Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb recall: Due to out-of-specification, or potential out-of-specification
Due to out-of-specification, or potential out-of-specification, levels of endotoxins
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Class II · 4 months ago
Boston Scientific Corporation CRE Pro Wireguided 12-15mm 240cm recall: Potential sterile breach of the pouches in which devices are packaged
Potential sterile breach of the pouches in which devices are packaged.
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Class II · 4 months ago
Medline Convenience kits containing recalled Swan-Ganz Catheters recall: Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue)…
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Class II · 4 months ago
Bard Access Systems, Inc. CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI recall: Due to lidocaine ampoules being manufactured under deficient manufacturing
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
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Class II · 4 months ago
Raysearch Laboratories Ab RayCare 2024A SP1. Oncology Information Systems recall: Beam set delivery note issues in which there is potential data loss
Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is…
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Class II · 4 months ago
Medline Convenience kits containing recalled Swan-Ganz Catheters KIT recall: Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue)…
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Class II · 4 months ago
Remel, Inc GC Agar Base 10/PK R04030 recall: Reduced or no recovery of some strains of Neisseria gonorrhoeae
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
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Class II · 4 months ago
Boehringer Ingelheim Pharmaceuticals, Inc. Synjardy XR Tablets , 12.5/1000 mg recall: CGMP Deviations: An incorrect detergent was used and the required swab
CGMP Deviations: An incorrect detergent was used and the required swab sampling was not performed on a production hopper that had previously been…
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Class II · 4 months ago
Lannett Company Inc. Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate recall: Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets
Labeling: Label Mix-up: Capsules contain only immediate-release (IR) pellets while labeled as ER capsules.
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Class II · 4 months ago
CareFusion 213, LLC BD ChloraPrep Clear, , and 70% v/v isopropyl alcohol recall: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead…
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Class II · 4 months ago
CareFusion 213, LLC BD ChloraPrep Hi-Lite Orange recall: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead…
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Class II · 4 months ago
CareFusion 213, LLC BD ChloraPrep Scrub Teal, and 70% v/v isopropyl alcohol) packaged recall: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead…
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Class II · 4 months ago
McKesson Gemcitabine Injection, 1 g per 26.3 mL , 26.3 mL Single-Dose Vial recall: Temperature Abuse: Product was stored incorrectly in a controlled room
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
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Class II · 4 months ago
CareFusion 213, LLC BD ChloraPrep Hi-Lite Orange recall: Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep
Lack of assurance of sterility: Unsterilized ChloraPrep & PurPrep Applicators, intended for further processing and sterilization were instead…
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Class II · 4 months ago
Blaine Labs Inc Terpenicol Antifungal Cream , 1.0 oz bottles recall: CGMP Deviations; the firm discontinued required stability testing
CGMP Deviations; the firm discontinued required stability testing for products on the market still within expiry
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Class II · 4 months ago
Blaine Labs Inc Trifluent Pharma Tridergel Wound Care Gel, , 1.0 fl oz recall: CGMP Deviations: product manufactured in the same facility under the same
CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated
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Class II · 4 months ago
Accord Biopharma Inc Imuldosa, Injection, 130 mg/26 mL recall: Lack of assurance of Sterility
Lack of assurance of Sterility: