ProgenaCare recalls progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x 2 cm; (2) PM3002, 2 x 2 cm; (3)…
Inner pouch seal may be inadequate resulting in lack of sterility.
Read the official notice →- Date
- 2022-06-01
- Country
- United States
- Brand
- ProgenaCare
- Product
- progenamatrix Human Keratin Matrix, sterile, Rx, with the following model numbers: (1) PM2012, 12 x 2 cm; (2) PM3002, 2 x 2 cm; (3)…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, GA, FL, TN, and TX. There was…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
Other drugs & medical recalls in the United States
- 2022-06-08
US- 2022-06-02
- US
Asweets Recalls Wood Baby Activity Push Walkers Due to Strangulation Hazard
Rubber rings on the rear wheels can separate from the wheels and detach from the Activity Walkers, posing a strangulation hazard to young children.
- 2022-06-01
- US
MEDLINE INDUSTRIES, LP - Northfield recalls ABX Pentra Calcium AS CP, Reagent 90 mL, REF A11A01954
Product was shipped from a Medline warehouse to a customer at room temperature instead of refrigerated (ice). If affected product is used, the results from this impacted Calcium reagent will not be provided due to…
- US
Umano Medical, Inc. recalls AC-powered adjustable medical beds with built-in electric DC actuators and controls.
There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.
FDA · DeviceUmano Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of CA, PA,…Official notice → - US
ConvaTec, Inc recalls SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.
Firm received 10 complaints of skin barrier delamination issues (e.g. flange lifts from wafer, skin barrier layers separate) or tape border rips/tears.
FDA · DeviceConvaTec, IncDistributed nationwide to NJ, PA, OH, CA, AL, MI, NY, TX, FL, NC, VA, LA, IL,…Official notice → - US
Smith & Nephew Orthopaedics GmbH recalls INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Right nails were anodized, marked, and labelled as left nails and vice versa
FDA · DeviceSmith & Nephew Orthopaedics GmbHDistributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and…Official notice →