Connecticut recalls

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.

The CGuard Prime Carotid Stent System (model CND1040, 10mm×40mm) may encounter complications during deployment, including high resistance or inability to deploy the stent properly. This affects 211 units manufactured between February 3 and February 23, 2026, distributed across the United States.

The CGuard Prime Carotid Stent System (model CND1030, 10mm x 30mm) may be difficult or impossible to deploy during surgery due to complications in the delivery system. This affects 114 units manufactured between February 3 and February 23, 2026. No injuries have been reported.

The CGuard Prime Carotid Stent System (model CND0940, 9mm × 40mm, 135cm length) may experience difficulty during placement in the artery. The delivery system could encounter high resistance or fail to deploy the stent properly.

The CGuard Prime Carotid Stent System (model CND0930, 135cm) may experience complications during deployment that could result in high resistance or inability to place the stent. This affects 147 units manufactured between February 3, 2025 and February 23, 2026, distributed nationwide.

The CGuard Prime Carotid Stent System (model CND0840, 8mm×40mm) may experience high resistance or fail to deploy properly during the placement procedure. This affects 424 units manufactured between early February 2025 and February 2026.

InspireMD's CGuard Prime Carotid Stent System (model CND0830, 8mm×30mm) may experience complications during deployment that could make it difficult or impossible to place the stent. About 190 units were distributed nationwide between February 2025 and February 2026. No injuries have been reported so far.

The outer knife on certain D.O.R.C. TDC VELOCE 27G surgical cutters may become loose during use. This surgical device is used in ophthalmic (eye) procedures, and a loose knife could affect device performance.