Paragon 28, Inc. recalls Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
Suture anchor may break upon insertion, which could lead to potential debris in patient, and delays in surgery.
Read the official notice →- Date
- 2022-09-28
- Country
- United States
- Brand
- Paragon
- Product
- Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture Anchor System
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AZ, IN, LA, NJ, TX, WA, NY, MD,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Paragon recalls
- 2026-08-26
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- 2026-07-29
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FDA · DeviceParagon 28, Inc.US nationwide, Australia, Canada, The Netherlands, and New ZealandOfficial notice → - 2025-12-10
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Medical devices distributed, prior to sterilization
- 2022-08-03
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Due to Titanium plasma coating not present implant.
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Other drugs & medical recalls in the United States
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CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
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Viatris Inc recalls Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan…
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SUN PHARMACEUTICAL INDUSTRIES INC recalls Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories…
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
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