Tag: huons_co_ltd

Argon Medical Issues Class I Recall for Kits with Huons Lidocaine

30 Jul 2026 12:41 p.m. · Source: US Food and Drug Administration

Argon Medical issued a Class I recall for convenience kits containing Huons lidocaine, citing risks like infection and meningitis. The FDA warns of serious injury or death if uncorrected, with two serious injuries reported.

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FDA Announces Class I Recall for Arrow International Convenience Kits

16 Jul 2026 1:03 p.m. · Source: US Food and Drug Administration

Arrow International has issued a Class I recall for convenience kits containing Huons-manufactured lidocaine, bupivacaine, and saline ampules. The FDA warns of serious injury or death if uncorrected, citing risks like infection and ineffective pain control from the compromised injectables.

Health Business Medical Science Legal Economy Product Recall Medical Devices Arrow International Huons Co. Ltd FDA Lidocaine Bupivacaine Food Recalls Drugs
B. Braun Recalls Spinal Anesthesia Kits Due to Huons Bupivacaine Recall

16 Jul 2026 10:58 a.m. · Source: US Food and Drug Administration

B. Braun Medical, Inc. has recalled spinal anesthesia kits containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, due to serious risks including infection and meningitis. The FDA has classified this as the most serious type of recall.

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FDA Warns Against Use of Recalled Bupivacaine Injections from Huons Co., Ltd.

12 Jun 2026 1:31 p.m. · Source: US Food and Drug Administration

Huons Co., Ltd. has recalled Bupivacaine Hydrochloride in Dextrose Injection, USP, due to quality issues. Medline advises customers to remove these injections from convenience kits, as their use poses risks of infection, inflammation, and severe neurological complications.

Health Business Politics and Government Medical Science Federal Government Legal General Politics Bupivacaine Hydrochloride Huons Co., Ltd.Medline FDA Product Recall Medical Devices Drug Safety Food Recalls Drugs
Becton Dickinson Issues Correction for Spinal Trays with Bupivacaine Ampules

4 Jun 2026 10:37 a.m. · Source: US Food and Drug Administration

Becton Dickinson is correcting BD Spinal Trays by removing bupivacaine ampules due to quality issues and potential ineffectiveness. The FDA deems this a serious recall, warning of risks like infection or reduced anesthetic effect.

Health Business Politics and Government Medical Science Federal Government Economy Becton Dickinson BD Spinal Trays Bupivacaine Huons Co. Ltd.FDA Product Recall Anesthesia Food Recalls Drugs

Tag: huons_co_ltd

Argon Medical Issues Class I Recall for Kits with Huons Lidocaine

FDA Announces Class I Recall for Arrow International Convenience Kits

B. Braun Recalls Spinal Anesthesia Kits Due to Huons Bupivacaine Recall

FDA Warns Against Use of Recalled Bupivacaine Injections from Huons Co., Ltd.

Becton Dickinson Issues Correction for Spinal Trays with Bupivacaine Ampules