Fresh Recalls

Medline Convenience Kits: recall status

⚠ Recalls found. Medline Convenience Kits is named in 77 official recalls in our current data:

Brand
Medline Industries
Also listed as
Medline convenience kits

Recalls naming this model

FDA Class II · Medical device · July 15, 2026

Medline Convenience Kits recall — Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2695-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Medline Convenience Kits recall — Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2696-2026 · Official record ↗

FDA Class II · Medical device · July 15, 2026

Medline Convenience Kits recall — Medline Industries, LP

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm ge…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2697-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2533-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2534-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2535-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2536-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2537-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2538-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2539-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2540-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2541-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2542-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2543-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2544-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2545-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2546-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

Medline Convenience Kits recall — Medline Industries, LP

The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to qu…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2547-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2452-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2453-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2454-2026 · Official record ↗

FDA Class I · Medical device · July 1, 2026

Medline Convenience Kits recall — Medline Industries, LP

The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were rec…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2455-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2418-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2419-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2420-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2421-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2422-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2423-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2424-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2431-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2432-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2433-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2434-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2435-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2436-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2438-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2439-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2440-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2441-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2442-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2443-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2444-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2445-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2446-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

Medline convenience kits recall — Medline Industries, LP

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Company / brand: Medline Industries

Affected product: Medline convenience kits

Official ID Z-2447-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2089-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2090-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2091-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2092-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2094-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2095-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2096-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2100-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2102-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2103-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2104-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2105-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2106-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2107-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2108-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2110-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2111-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2112-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2113-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2115-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2116-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2117-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2118-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2119-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2120-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2121-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2122-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2123-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2124-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2125-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2126-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Medline Convenience Kits recall — Medline Industries, LP

Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…

Company / brand: Medline Industries

Affected product: Medline Convenience Kits

Official ID Z-2127-2026 · Official record ↗

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Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.