Medline Medical Kits Recalled for Leaking Isopropyl Alcohol
Medline convenience kits containing leaking bottles of isopropyl alcohol are being recalled. Approximately 477 units were distributed nationwide and should not be used.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is a Class II FDA recall for medical kits with leaking isopropyl alcohol, presenting a risk of chemical exposure and potential skin or eye contact. No illnesses or injuries have been reported in the source text, so the score is 3 per the rubric for risk-of-harm products without reported harm.
Plain-English summary
Medline Industries is recalling certain convenience kits labeled as MIDDLE EAR PACK-LF (Model DYNJ0689093V) and EENT PACK (Model DYNJ62927) because they contain leaking bottles of isopropyl alcohol.
Approximately 477 units were distributed throughout the United States. Affected lot codes include 22DMI666, 21LBI103, 21HBO705, 21JBP781, 21JBQ762, 21FBG532, and 21FBG535 for the MIDDLE EAR PACK-LF, and 22BBB412 for the EENT PACK.
Healthcare facilities and individuals who have received these kits should stop using them immediately and contact Medline Industries to arrange for replacement or return of the affected products.
The recalled product
- Product
- Medline convenience kits labeled as: a. MIDDLE EAR PACK-LF, Model DYNJ0689093V, b. EENT PACK, Model Number DYNJ62927 Model/Catalog Number: a. DYNJ0689093V, b. DYNJ62927
- Manufacturer
- MEDLINE INDUSTRIES, LP - SPT
- Category
- Medical Device
- Affected units
- 477
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 (10)
- Lot Code: a. Model Number DYNJ0689093V
- Lot Codes: 22DMI666
- 21LBI103
- 21HBO705
- 21JBP781
- 21JBQ762
- 21FBG532
- 21FBG535
- b. Model Number DYNJ62927
- Lot Numbers: 22BBB412
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 8 recalled by MEDLINE INDUSTRIES, LP - SPT under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 8 products in this recall →Related recalls
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