FDAMarch 24, 2023device
FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the endoscope.
What to do
FDA enforcement status: Ongoing
Brands named
richard wolfrichard
UPCs
04055207020265
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAPiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).2025-04-09
- CPSCWolf Appliance Recalls Dual Fuel Ranges with Infrared Griddles Due to Burn and Fire Hazards2024-11-07
- FDAHenke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial injection of liquids or diluted drugs in combination with an adequate medical device or for withdrawal of fluids from the body. Ref: 4100.000V02023-07-27
- FDAFLEX. BIOPSY FORCEPS 5FR WL 550MM, Product Number 829.0512023-03-24
- FDAFLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.6852023-03-24
- FDAFLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 828.0512023-03-24
- FDALake Wolf Creamery Queso Fresco, crumbling fresh cheese, refrigerated, vacuum packaged in flexible plastic packages, net wt. 1.5 lbs. or 0.5 lbs. No UPC.2021-09-30
- FDALake Wolf Creamery Queso Oaxaca, ribbon cheese, refrigerated, vacuum packaged in flexible plastic packages, net wt. 3 lbs., 2 lbs., 1.5 lbs., and 0.5 lbs. No UPC.2021-09-30
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