Kit: Midline Insertion DA. MAI Kit Part Number: 77981B
Check against the official notice below — it lists the full affected range.
Medical Action Industries, Inc. is recalling its 306 Kit: Midline Insertion DA (Kit Part Number 77981B) due to a potential breach in the package integrity of a component called the BD ChloraPrep 3mL applicator. The recall affects 110 cases (containing 5 kits per case) that were distributed nationwide to Ohio, Oregon, Florida, and California. The affected kits are identified by UDI (GTIN) 20809160284053 and have lot numbers 0000281502, 0000282039, 0000274390, or 0000279101, with expiration dates ranging from July 9, 2021 to April 8, 2022.
The source document does not specify a remedy or what action affected consumers should take.
Written by software from the official notice below. Not reviewed by a lawyer.
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Reason for recall: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Distribution: Distributed US nationwide to OH, OR, FL and CA. Quantity: 110 cases (5 kits per case) Lot/code info: Kit Number: 77981B; UDI (GTIN): 20809160284053; Lot Number: 0000281502 (Expiration Date: 04/08/2022), 0000282039 (Expiration Date: 04/08/2022), 0000274390 (Expiration Date: 07/09/2021), and 0000279101 (Expiration Date: 11/13/2021)
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.