Spectra Lidocaine HCl Injection Recall
Spectra Medical Devices is recalling Lidocaine HCl Injection because the company cannot guarantee the product is sterile. Non-sterile injectable medications can …
Spectra Medical Devices, Llc
Spectra Medical Devices, Llc Recalls (2026)
Every recall we are tracking for Spectra Medical Devices, Llc, newest first, sourced from the FDA. If you are wondering whether your Spectra Medical Devices, Llc product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Spectra Medical Devices, Llc recall posts.
1 recall · updated May 12, 2026
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Chiesi USA is recalling CLEVIPREX (clevidipine) injectable emulsion vials because the manufacturer cannot assure the product remains sterile. This injectable …
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QC Quality Choice Carbamide Peroxide Recall
QC Quality Choice Carbamide Peroxide 6.5% oral rinse is being recalled because it is sub-potent: it contains far less active ingredient than labeled (about 0.6% …
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Clinere Carbamide Peroxide Recall
Clinere Carbamide Peroxide ear drops are significantly weaker than labeled and have an unusually low pH, reducing effectiveness and potentially causing …
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Lupin Glucagon Emergency Kit Recall
Lupin Pharmaceuticals is recalling Glucagon Emergency Kits due to a manufacturing defect that may affect the syringe's ability to inject properly. If you rely …
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BD ChloraPrep Hi-Lite Orange Recall
BD ChloraPrep Hi-Lite Orange applicators (a skin antiseptic) were distributed without proper sterilization assurance. These products should have been sterilized …
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Methohexital Sodium Injection Recall
Methohexital Sodium for Injection 500 mg multiple dose vials made by OneSource Specialty Pharma have failed quality tests for impurities and degradation. …
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