Medshape, INC. recalls DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
The firm identified a nonconformance in Lot 04882 involving the endcap being manufactured to a longer length than indicated in product specifications, introducing the risk of the +6 mm endcap not seating flush with the…
Read the official notice →- Date
- 2022-01-12
- Country
- United States
- Brand
- Medshape
- Product
- DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile
- Classification
- Class II
- Units
- Domestic: CA, FL, GA, IL, IN, MA, MD, TX, and WA.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Medshape recalls
- 2025-09-10
USMedshape, INC. recalls Medshape Universal Joints, REF: DNE-9000-UJ
Bone external fixation system may have the pin that can become dislodged resulting in frame instability, the use of this product may cause a delay in surgery or a revision if the device is use.
FDA · DeviceMedshape, INC.US Nationwide distribution in the states of CA, IL, NJ, TX, FL, IN, OH, WI,…Official notice →
Other drugs & medical recalls in the United States
- 2022-01-12
- US
Nikkiso Ltd - Shizuoka Plant recalls DBB-06 Hemodialysis Delivery System
Device lacks premarket approval.
FDA · DeviceNikkiso Ltd - Shizuoka PlantDistributed nationwide to NY, MO, WA, CA, and TN.Official notice → - US
Qiagen Sciences LLC recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA EUA 200075); REF 691223
The firm identified sixteen (16) faulty cartridges in LOT 210209, which contain incorrect primer-probe mixes in the reaction chambers. If an affected cartridge is used, false-negative, false-positive, or both…
FDA · DeviceQiagen Sciences LLCDomestic distribution to AL, DC, KY, MD, ME, NJ, OK< PA, and TX. No foreign…Official notice → - US
Tapemark Company recalls iontoPATCH On-the-Go Patch Therapy, Transdermal Iontophoretic Drug Delivery System, Extra Strength, 8-HOUR Average Wear Time, 6/1-patch…
The dosage information on the pouch is incorrect; the primary carton label is correct.
FDA · DeviceTapemark CompanyUS Nationwide distribution in the states of CA, FL, IL, MO, NY, OH, and TN.Official notice → - US
Biomeme, Inc. recalls Biomeme SARS-CoV-2- Real Time RT-PCR Test, Instructions for Use, Part number 100002824 Subcomponent of: SARS-CoV-2 Go-Strips, 3000555;…
The current IFU specifies a shelf-life of one week after resuspension of the RPC Buffer when stored at room temperature. Ongoing stability studies have indicated the need to shorten the life of the RPC Buffer once…
FDA · DeviceBiomeme, Inc.Domestic distribution to AZ, CA, FL, HI, IN, KY, MD, MO, NC, NJ, NY, OH, OK,…Official notice → - US
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An automated, clinical chemistry analyzer designed to…
(1)Software (SW) versions V1.25.1 and lower may result in TDef (Test Definition) Parameters for Open Channel Assays reverting to Default Value would shift test results by the magnitude of the implemented Assay…
FDA · DeviceSiemens Healthcare Diagnostics, Inc.Nationwide Foreign: AU DE AE TR BG CL IN CZ BR ES KE CN PL SA BE IQ IT CW SE…Official notice → - US
Flower Orthopedics Corporation recalls Flex-Thread Inserter Shaft intended for Fibula intramedullary-intended to be used with the Inserter Draw Rod and Blue Ratchet…
Mating incompatibility between the Inserter Shaft and the Inserter Draw Rod causing the inserter draw rod to bind and not rotate freely as intended surgeon may be unable to complete surgery unless a second set is…
FDA · DeviceFlower Orthopedics CorporationUS Nationwide distribution in the states of AZ, CA, CO, GA, TN, FL, IL, MA,…Official notice →