LIDOLOG KIT Lidocaine HCl Injection, USP 2%, 40 mg/2 mL (20 mg/mL), 2 mL per Single-Dose recall — FDA D-0552-2026
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Complete FDA and NHTSA recall records dated in June 2026.
These records include useful source details for the selected month.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Contains statement does not declare Almond
Contains statement does not declare Walnut
Product is potentially contaminated with foreign material (plastic particles).
Imported Enoki Mushrooms samples collected by Florida Department of Health tested positive for Listeria Monocytogenes.
Possible contamination with Cereulide toxin.
Undeclared egg
Contains statement does not declare Crab
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Contains statement does not declare Hazelnut
Contains statement does not declare Crab and Pollock
Contains statement does not declare Salmon
Potential contamination with foreign objects (metal pieces).
Potential contamination with Salmonella
The product may contain undeclared allergens (cashews, pistachios), and dried cherries.
Potential contamination with foreign objects (metal pieces).
Contains statement does not declare Shrimp
Contains statement does not declare Tuna
Potential contamination with foreign objects (metal pieces).
Product contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination
Possible carbon steel foreign material (1-2mm)
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
Salmonella. The firm was notified by the North Carolina Department of Agriculture that the product test positive for Salmonella.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.