HIGH

Medline Recalls Medical Kits Over Seal Integrity Issues

Medline Industries, LP recalled 7,380 medical convenience kits on December 24, 2025. The recall affects the PowerGlide Dressing Change Kit and Central Line Tray with ChloraPrep swabsticks. An open seal on packaging may compromise sterility and patient safety.

Quick Facts at a Glance

Recall Date
December 24, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

The recall includes two specific kits: PowerGlide Dressing Change Kit (SKU DYNDH1576) and Central Line Tray with ChloraPrep SWB (SKU RWM-DC57KC). These kits were distributed nationwide in the U.S.

The Hazard

BD ChloraPrep Triple Swabsticks in the kits may have an open seal, potentially compromising sterility. This defect poses a high risk to patient safety.

Reported Incidents

No injuries or incidents have been reported related to this recall. However, the potential for compromised sterility raises serious concerns.

What to Do

Stop using the recalled medical kits immediately. Follow instructions provided by Medline Industries, LP, or your healthcare provider.

Contact Information

For assistance, contact Medline Industries, LP. Visit their website or call the customer service number provided in the recall notification.

Key Facts

  • Recall date: December 24, 2025
  • Quantity recalled: 7,380 kits
  • Affected SKUs: DYNDH1576, RWM-DC57KC
  • Open seal issue compromises sterility
  • No reported injuries yet

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
Kit SKU DYNDH1576
UDI/DI 10193489437041
Lot Number 25EBP737
Kit SKU RWM-DC57KC
UDI/DI 10889942582013
+1 more
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

Related Recalls

HIGH

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding
Lack of
Read more
HIGH

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Violations

Pro Numb Tattoo Numbing Spray was recalled on February 2, 2026 due to cGMP deviations. The product, containing 4% lidocaine, is distributed by Pro Numb Tattoo Numbing Spray LLC. Consumers should stop using it immediately and contact the company for further guidance.

PRO NUMB SENSITIVE SKIN
cGMP deviations
Read more