Medline Recalls Hip Scope Packs Due to Removal Difficulties
Medline Industries is recalling 56 hip scope packs because they are difficult to remove and leave adhesive residue on patient skin.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: The source describes the hazard as the product being difficult to remove and leaving adhesive residue on skin. The source does not report any illnesses, injuries, or deaths.
Plain-English summary
Medline Industries, LP is recalling 56 units of MEDLINE medical convenience kits labeled as HIP SCOPE PACK. The affected products include Medline Kit Number/SKU DYNJ64103C and DYNJ64155B. The recall covers specific lot numbers and UDI/DI codes as detailed in the agency record.
The recall was initiated due to reports that the product is difficult to remove from patients and leaves adhesive residue on the patient's skin. The source text does not report any illnesses, injuries, or deaths associated with these products.
The affected kits were distributed worldwide, including in the United States, Canada, Turkey, Australia, and the United Arab Emirates. Consumers and healthcare providers should stop using the affected products and contact Medline Industries for further instructions.
The recalled product
- Product
- MEDLINE medical convenience kits labeled as: 1) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64103C; 2) HIP SCOPE PACK, Medline Kit Number/SKU DYNJ64155B.
- Manufacturer
- Medline Industries, LP
- Category
- Medical Device — Surgical Kits
- Affected units
- 56
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 (8)
- Medline Kit Number/SKU DYNJ64103C
- UDI/DI 10198459221828 (each) 40198459221829 (case)
- Lot Number 26ABI361
- Lot Number 25KBD396
- Medline Kit Number/SKU DYNJ64155B
- UDI/DI 10198459146954 (each) 40198459146955 (case)
- Lot Number 26ABP213
- Lot Number 25LBJ299.
Distribution
Distributed nationwide across the United States.
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