NA
Fehling Instruments GmbH & Co. KG · Model BOP-2 · UDI-DI 04058749007183
LRW
Prescription
10
510(k) clearances
795
Adverse events (1 deaths)
20
Recalls
514
Facilities
Description
CERAMO TC POTTS vessel scissors, 45° angled, 190 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-11-13 | Medline Industries, LP | The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized. |
| 2025-11-13 | Medline Industries, LP | The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized. |
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-10-21 | MEDLINE INDUSTRIES, LP - Northfield | Tip protector may fall off within the packaging, resulting in compromised sterile barrier system and loss of sterility. |
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
| 2023-11-16 | Steris Corporation | Bandage Scissors handle cover component contains an incorrect color masterbatch resin carrier. This may allow a pink dye/residue to appear on the Bandage Scissors and/or sterilizat |
| 2022-07-25 | Stradis Medical, LLC dba Stradis Healthcare | The sterile barrier may be compromised. |
| 2018-06-12 | Teleflex Medical Europe Ltd | The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.