McKesson LiquiBand Exceed Skin Adhesive Storage Temperature Exposure Recall
McKesson is recalling LiquiBand Exceed skin adhesive products nationwide due to facility temperature excursions between June and August 2021. The FDA states the affected products are not likely to cause adverse health consequences.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class III recall with no reported illnesses or injuries. The source explicitly states the device 'is not likely to cause adverse health consequences,' making the hazard theoretical. The recall is precautionary in nature, driven by storage condition deviations.
Plain-English summary
McKesson Medical-Surgical Inc. is recalling three models of LiquiBand Exceed skin adhesive due to facility temperature excursions that occurred between June and August 2021. These temperature deviations may have impacted product effectiveness.
The affected products include the 0.4 mL Liquid Dome Applicator Tip (Model 122-LBXS), the 0.8 mL Liquid Precision and Dome Applicator Tip (Model 122-LBX), and the Tissue Flow Tip 0.5 mL (Catalog #122-LFC). All products distributed to healthcare facilities nationwide between June 1 and September 30, 2021 are included in this recall.
The FDA has determined that devices with this specific storage temperature deviation are not likely to cause adverse health consequences.
The recalled product
- Product
- a. Skin Adhesive McKesson LiquiBand Exceed 0.4 mL Liquid Dome Applicator Tip 2-Octyl Cyanoacrylate. Model Number: 122-LBXS. b. Skin Adhesive McKesson LiquiBand Exceed 0.8 mL Liquid Precision and Dome Applicator Tip 2-Octyl Cyanoacrylate. Ref: 122-LBX. c. ADVANCED MEDICAL SOLU
- Manufacturer
- Mckesson Medical-Surgical Inc. Corporate Office
- Hazard
- temperature-exposure
- loss-of-effectiveness
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- a. UDI-DI :10612479232256
- 40612479232271
- 20612479195978
- 40612479195989. c. GTIN: 20612479185863
- 10612479208206
- 40612479185874
- 20612479185863
Distribution
Distributed nationwide across the United States.
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