Critical Alert
Medline Industries Recalls MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-2747-2026Medical Device
Medline Industries Recalls MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
Medline Industries, LP · Class I — Most Serious
Product Description
MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
Reason for Recall
Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. was notified by their supplier, Spectra Medical Devices, LLC of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. Huons Co, Ltd. has issued a voluntary recall of this product due to quality issues.
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US: OH, CA, IL, IN, FL, SC, AZ, NJ.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class I recall — the FDA's most urgent classification — has been issued for a medical device recalled by Medline Industries, LP on June 5, 2026. Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in Dextrose Injection, USP. B. Braun Medical Inc. This recall affects 60 kits and was distributed in US: OH, CA, IL, IN, FL, SC, AZ, NJ. Class I recalls indicate a reasonable probability of serious health consequences or death. Consumers should stop using this product immediately.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects and Medline Industries recalls.