South Carolina recalls

Boston Scientific has recalled certain CSK Electrode models used in neuromodulation procedures because they may not perform reliably as intended. The affected electrodes come in multiple configurations and lengths. No injuries have been reported to date.

Some units of Inter-Med's Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (catalog 504600-28) contain the package insert for Ferric Sulfate Gel instead. The wrong insert gives incorrect first aid instructions—specifically, it tells users to induce vomiting if the gel is swallowed, when the correct instructions say not to induce vomiting.

DT MedTech discovered that some Hintermann Series Talar Implant units labeled as left implants actually contained right implants inside the packaging. This mix-up was found through customer complaints. A total of 67 units across five US states and two countries are affected.

Three lots of Siemens Dimension Tacrolimus Flex Reagent Cartridges show a potential positive bias in quality control and patient test results. This means the cartridges may report tacrolimus levels that are higher than actual values. The affected lots are FA6254, FA6260, and FA6286.

The EXENT Analyser, an automated blood-test device, has a software issue where certain test plates were marked as passed without performing required quality checks. This could allow inaccurate M-protein measurements—either missed detections or wrong concentration values—to be reported to clinicians.

Medartis has recalled certain APTUS 5.0 headed cannulated compression screws (CCS) used in bone fixation surgery because the central hole in the screw is not properly centered. This affects 13 units across five states. No injuries have been reported.

Sagemax Bioceramics is recalling NexxZr T Multi A3.5 W98-16mm zirconium oxide discs used in dental crowns and bridges. Some discs may have a reduced or missing dentin layer, which can weaken them and cause fractures when patients chew or bite.

When using two or four amplifiers together in certain configurations, the SD LTM 64 PLUS may display a 1-second timing delay between channel blocks. This delay could cause doctors to misinterpret EEG test results. The issue affects devices running specific firmware versions.

Avanos Medical included lidocaine hydrochloride injections with quality issues in their MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) kits. The lidocaine was subject to a supplier recall for quality defects. About 1,205 kits across the US were affected.

Avanos Medical included lidocaine hydrochloride injections with quality issues in their MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) kits. The lidocaine was subject to a supplier recall for quality defects. About 6,000 kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injections with quality issues in sterile PEG (feeding tube) kits. The lidocaine was subject to a supplier recall for manufacturing defects. About 218 kits with specific lot numbers were affected nationwide.

Avanos Medical included lidocaine hydrochloride injections with quality defects in 234 sterile PEG kits. The injections were already the subject of a supplier recall. The kits affected are model 8170-24 in specific lot numbers distributed nationwide.

Avanos Medical included lidocaine hydrochloride injections with quality issues in certain sterile PEG (feeding tube) kits. The lidocaine was subject to a supplier recall for manufacturing defects. About 1,615 kits with specific lot numbers were affected nationwide.

Avanos Medical included lidocaine hydrochloride injection from a recalled supplier in sterile feeding tube kits. The supplier had recalled the lidocaine due to quality issues. Approximately 53 kits with lot number 30370718 were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injections with quality issues in their MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) kits. The lidocaine was subject to a supplier recall for quality defects. Approximately 1,006 kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injection from a supplier recall into sterile PEG (feeding tube) kits due to quality issues with the lidocaine. The affected kits are the MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr, with specific lot numbers ranging from 30371313 to 80403340.

Avanos Medical included lidocaine hydrochloride injections with quality issues in sterile PEG (feeding tube) kits. The lidocaine was subject to a supplier recall due to manufacturing problems. About 208 kits with specific lot numbers were affected.

Avanos Medical included lidocaine hydrochloride injections with quality issues in certain MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) feeding tube kits. The lidocaine was subject to a supplier recall due to manufacturing or quality problems. About 132 kits with specific lot numbers were affected.

Avanos Medical's MIC Safety Percutaneous Endoscopic Gastrostomy (PEG) Kit 20 Fr includes lidocaine hydrochloride injection from a supplier that issued a recall due to quality problems. The affected kits were distributed nationwide; no injuries have been reported so far.

Avanos Medical included lidocaine hydrochloride injection with quality defects in 22 sterile feeding tube kits. The lidocaine was subject to a supplier recall for quality issues. The affected kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injection with quality issues in CORFLO Safety PEG feeding tube kits. The lidocaine was subject to a supplier recall and should not have been distributed in these sterile kits. The affected kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injection from a recalled supplier into 43 CORFLO Safety PEG Kits. The lidocaine had quality issues that could affect the sterility or safety of the kit. The affected kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injections with quality problems into 72 sterile CORFLO Safety PEG Kits. The lidocaine was subject to a supplier recall for manufacturing defects. The affected kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injection from a supplier recall into 49 sterile CORFLO Safety PEG kits. The lidocaine was recalled by its supplier due to quality issues. Affected lot numbers are 30365230, 30367013, and 30373825.

Avanos Medical included lidocaine hydrochloride injection in sterile kits. The lidocaine was subject to a supplier recall due to quality issues. The affected kits were distributed nationwide.

Avanos Medical included lidocaine hydrochloride injection in CORFLO Safety PEG Kits that was subject to a supplier recall due to quality issues. The affected kits were distributed nationwide. No injuries have been reported.

Avanos Medical included lidocaine hydrochloride injection with quality issues into CORFLO Safety PEG Kit sterile sets. The lidocaine was subject to a supplier recall for manufacturing defects. Sixty-one kits with six lot numbers were affected.

Avanos Medical included lidocaine hydrochloride injections with quality issues in 231 CORFLO Safety PEG Kits (model 30-4320). The lidocaine itself was recalled by its supplier due to manufacturing problems. The affected kits were distributed nationwide.

SporeTraq Mail-In Spore Testing Service kits were processed with incorrect incubation times, which may affect the accuracy of sterilizer efficacy test results. The kits are used by healthcare facilities to verify that their sterilization equipment is working properly.

HF Acquisition Co LLC is recalling the SporeTraq Mail-In Spore Testing Service (52 tests) because some test strips were not incubated for the correct length of time. The test strips are used by healthcare facilities to verify that their sterilization equipment is working properly. Incorrect incubation times can produce unreliable test results.