Penner Pacific Bathing Spa Recall
Penner Pacific Bathing Spa Model 360020-1P is being recalled because it lacks a unique device identifier required by regulation. This is a labeling and tracking …
Penner Patient Care, Inc.
Every recall we are tracking for Penner Patient Care, Inc., newest first, sourced from the FDA. If you are wondering whether your Penner Patient Care, Inc. product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Penner Patient Care, Inc. recall posts.
1 recall · updated Aug 13, 2025
Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the manifold. This can …
Boston Scientific Corporation
Boston Scientific is replacing certain FARASTAR Pulsed Field Ablation generators that cannot work with the FARAPOINT catheter. If your generator has an …
Boston Scientific Corporation
The Faradive Steerable Sheath Clear used in cardiac catheterization procedures may allow air to enter the bloodstream if the dilator is inserted incorrectly …
Boston Scientific Corporation
ChloraPrep FREPP sterile skin antiseptic applicators were distributed without proper sterilization, posing a risk of infection. These applicators are used …
CareFusion 213, LLC
Orthofix MINIRAIL external fixation devices were shipped with incorrect model labels. The M101 was labeled as M103, the M103 was labeled as M101, and the M122 …
Orthofix U.S. LLC
ConvaTec is recalling Aquacel Ag Surgical SP surgical dressings (REF 413556, 9cm x 15cm size) because some were made thicker than the design specification. The …
ConvaTec, Inc
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