Endo Pharmaceuticals Issues Voluntary Nationwide Recall for Two Lots of Robaxin® 750mg Tablets 100 Count Bottle Packs Due to Incorrect Daily Dosing Information on Label
Patients who follow the directions on the bottle may experience significant drowsiness or dizziness which would put them at risk of falls or an overdose which could result in seizures, coma, or death. To date,
Robaxin® 750mg Tablets contain the active ingredient methocarbamol and are indicated as an adjunct therapy to rest, physical therapy and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. Robaxin® 750mg Tablets are packed in bottles of 100 tablets with package labeling featuring the product name, strength, lot number, expiry date and the National Drug Code number NDC 52244-449-10.
The recall includes the following product lots:
- Robaxin® 750mg, 100 Count Bottle pack, Lot 216702P1, Expiration Date:
September 2020 ; and - Robaxin® 750mg, 100 Count Bottle pack, Lot 220409P1, Expiration Date:
January 2021 .
No other lots of Robaxin® are affected by this market action.
Robaxin® 750mg 100 Count Bottle packs were distributed by wholesale distributors to retail pharmacies.
Distributors and retailers that have product which is being recalled should stop distributing and dispensing and return to the place of purchase.
Consumers in possession of any unused prescribed Robaxin® 750mg product bearing lot numbers 216702P1 or 220409P1 should discontinue use of the product and return the unused product by following the instructions below:
- Please contact Inmar at 1-866-391-0620, Monday through Friday (
9am to 5pm ET ) or email robaxin@inmar.comfor the following:- Product Return
- Upon contacting Inmar and indicating you have unused product, please expect Return Authorization labels and Shipping instructions.
- Product Reimbursement
- Upon contacting Inmar, please be prepared to share proof of purchase.
- Proof of purchase can be sent to robaxin@inmar.com or
635 Vine St. Winston Salem, NC 27101-Attention Recall Department , Robaxin Recall.
- Proof of purchase can be sent to robaxin@inmar.com or
- Upon contacting Inmar, please be prepared to share proof of purchase.
- Product Return
Distributors, retailers and consumers with questions regarding this recall can contact Inmar by telephone at 1-866-391-0620 during the following hours: Monday through Friday (
Adverse reactions or quality problems experienced with the use of this product may be reported to
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: use postage-paid, pre-addressed Form FDA 3500 available at: www.fda.gov/MedWatch/getforms.htm. Mail to address on the pre-addressed form or fax to: 1-800-
FDA -0178
This Product Recall is being made with the knowledge of the
About
Cautionary Note Regarding Forward-Looking Statements
Certain information in this press release may contain certain "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, and any applicable Canadian securities legislation. Statements including words such as "believes," "expects," "anticipates," "intends," "estimates," "plan," "will," "may," "look forward," "intend," "guidance," "future" or similar expressions are forward-looking statements. Because these statements reflect our current views, expectations and beliefs concerning future events, these forward-looking statements involve risks and uncertainties. Investors should note that many factors, as more fully described under the caption "Risk Factors" in
View original content to download multimedia:http://www.prnewswire.com/news-releases/endo-pharmaceuticals-issues-voluntary-nationwide-recall-for-two-lots-of-robaxin-750mg-tablets-100-count-bottle-packs-due-to-incorrect-daily-dosing-information-on-label-300720902.html
SOURCE
Endo International plc: Investors/Media: Laure Park, (845) 364-4862; Media: Heather Zoumas-Lubeski, (484) 216-6829