Medline

Medline Industries is recalling nine types of surgical convenience kits that contain BD PurPrep solution. The solution may be contaminated with low levels of Bacillus species, a bacterium that could pose a risk if the kits are used in sterile procedures. The recall affects specific lot numbers of joint, spine, and neurological surgery kits distributed to hospitals and surgical centers in ten U.S. states.

Medline Industries recalled specific NEURO PACK medical convenience kits because the included BD PurPrep 26 mL solution may contain low levels of Bacillus species bacteria. The contamination was identified in kits distributed to hospitals and medical facilities in 10 U.S. states.

Medline Industries is recalling three types of medical convenience kits (Shoulder Pack and Major Ortho Kit models) because the BD PurPrep solution included in them may contain low levels of Bacillus species bacteria. The contamination was discovered in specific lot numbers distributed across ten U.S. states.

Medline Industries is recalling specific pediatric open heart and cardiac surgical convenience kits that contain BD PurPrep solution potentially contaminated with low levels of Bacillus species. The affected kits were distributed to healthcare facilities in 10 states. No injuries have been reported.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could potentially be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled. The catheters contain increased amounts of raw material on the surface, which may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) include catheters with excess raw material on the surface. This material may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled due to increased raw material on the catheter surface. This contamination may cause staining and could potentially be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful to patients.

Medline convenience kits used in urology robotic procedures contain Bard Silastic Foley Catheters with excess raw material on the catheter surface. This material may cause staining and could potentially harm patients. The catheters were originally recalled by the manufacturer due to this manufacturing defect.

Medline convenience kits containing Bard Silastic Foley Catheters have been recalled because the catheters have an increased amount of raw material on their surface. This material may cause staining and could be harmful if the catheters are used.

Medline convenience kits containing Bard Silastic Foley Catheters (sizes 16, 18, and 20 French, 5cc balloons) have been recalled because the catheters have an increased amount of raw material on their surface. This contamination may cause staining and could be harmful if the catheters are used.

Medline medical procedure kits used for knee and hip surgeries contain pain management medications with quality issues that could make them less effective. The affected kits were distributed to hospitals and surgical centers in Missouri, Colorado, and Illinois.

Medline medical procedure convenience kits (model HIP CDS-LF) contain pain management medications with quality issues that could make the medication ineffective. The affected kits were distributed in Missouri, Colorado, and Illinois. No injuries have been reported.

Medline Industries is recalling specific surgical convenience kits used in joint replacement procedures because they contain a pain-reliever medication (Bupivacaine Hydrochloride in Dextrose) with quality problems. The medication was manufactured by Huons Co, Ltd. and distributed through B. Braun Medical. The quality issues were identified by the supplier and no injuries have been reported.

Medline Industries is recalling specific C-section convenience kits (SKU DYNJ910835 and DYNJ910835A) that contain an anesthetic medication with quality problems. The anesthetic, Bupivacaine Hydrochloride in Dextrose Injection, was recalled by its manufacturer due to quality issues.

Medline Industries is recalling specific Anterior Hip surgical kits (SKU DYNJ909640G) that contain a B. Braun convenience kit with Bupivacaine Hydrochloride in Dextrose Injection. The anesthetic component was manufactured by Huons Co, Ltd., which issued a voluntary recall due to quality concerns with the injectable drug.

Medline kits containing Zimmer Biomet mixing bowls and spatulas have seal defects that could compromise sterility during knee replacement surgery. The issue may require surgeons to obtain replacement equipment during the procedure, but no patient injuries have been reported.

Medline surgical kits containing Zimmer Biomet mixing bowls and spatulas have a seal defect that could compromise sterility. This defect could require surgeons to find an alternative device during a procedure. No injuries have been reported.

Specific lots of Medline reprocessed St. Jude Medical Response diagnostic electrophysiology catheters may contain small particles of residual material on surfaces that contact patients. If these particles dislodge during use, they could potentially cause blood clots, inflammation, or infection.

Medline Convenience kits contain Swan-Ganz catheters with a defective blue hub that can leak, break, or damage the lumen. This defect may cause leakage of medication, loss of blood, or infection during cardiac surgery.

Medline Convenience kits contain Swan-Ganz catheters with a defective blue hub on the proximal injectate lumen that can leak, break, or damage the lumen. This defect can lead to leakage during use, loss of medication, blood loss, or infection.

Medline's Convenience kits contain Swan-Ganz catheters that were recalled by manufacturer Becton Dickinson due to failures in the blue proximal injectate lumen hub. These failures can cause leaks, lumen damage, and breakage, which may result in infection, medication loss, or blood loss.

Medline Convenience kits contain Swan-Ganz catheters manufactured by Becton Dickinson (BD) that have a defect in the blue proximal injectate lumen hub. The hub can leak, break, or fail, potentially causing medication loss, blood loss, or infection during use.

Medline Convenience kits contain Swan-Ganz catheters manufactured by Becton Dickinson (BD) that may leak or break due to a defect in the blue proximal injectate lumen hub. The defect can cause leakage, lumen damage, breakage, and potential infection, medication loss, or blood loss during use.

Medline Convenience kits contain Swan-Ganz catheters that were recalled by manufacturer Becton Dickinson due to failures in the blue proximal injectate lumen hub. These failures can cause leaks, lumen damage, and breakage, potentially leading to infection, medication loss, or blood loss.

Medline Convenience kits contain Swan-Ganz catheters with a defective connector (blue hub) that can leak, break, or damage the internal lumen. This defect may lead to medication loss, blood loss, or infection during medical use.

Medline Convenience kits contain Swan-Ganz catheters with a defective blue hub that can leak, break, or damage the lumen. This defect may cause medication loss, blood loss, or infection during use.

Medline's Ophthalmic Pack with Lidocaine (Model DYNJ57922A) contains lidocaine ampules manufactured by Huons Co., Ltd. that have quality issues identified during an FDA inspection of the manufacturing facility. About 180 kits were distributed nationwide.