Calvin Scott & Company, Inc. recalls Benzonatate capsules, 100mg, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC…
Labeling: Label Mix-up: Bottle labeled as Benzonatate 100 mg capsules contained Benzphetamine 50 mg tablets and a bottle labeled as Benzphetamine 50 mg tablets contained Benzonatate 100 mg capsules.
Read the official notice →- Date
- 2022-06-01
- Country
- United States
- Brand
- Calvin Scott & Company, Inc.
- Product
- Benzonatate capsules, 100mg, repackaged in 30-count bottles, Distributed by Calvin Scott & Co., Inc, Albuq., NM. 87123, NDC 67877-0573-05
- Classification
- Class I
- Units
- 1 physician in Alpharetta, GA
- Category
- Drugs & medical
- Source
- FDA · Drug
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 Details may be shortened or out of date; the official notice is the authoritative source.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
- 2022-06-01
US
International Science & Technology, LP, DBA Diamatrix Ltd. recalls Outer Packaging Label: Protekt Sharps Safety Knives - REF: PG 44620MU, Sterile R, Multi-Use 2.2mm…
Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handles may contain a size of "2.5mm" when the actual size is "2.2mm".
FDA · DeviceInternational Science & Technology, LP, DBA Diamatrix Ltd.Worldwide distribution - US Nationwide distribution in the states of MN, TX…Official notice →US
Steris Corporation recalls Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5,000 per case 25 sleeves of 200 2 in x 2 in / 5.1 cm x 5.1 cm Model Number: ENC100
Product not approved for release for US distribution
US
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Sara Plus Active Floor Lift
The device may emit smoke or ignite.
FDA · DeviceARJOHUNTLEIGH POLSKA Sp. z.o.o.US Nationwide and Worldwide distributionOfficial notice →US
Olympia Compounding Pharmacy dba Olympia Pharmacy recalls Sodium Bicarbonate 8.4% MDV Injection, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy…
Lack of assurance of sterility.
FDA · DrugOlympia Compounding Pharmacy dba Olympia PharmacyDistributed Nationwide in th USA, Puerto Rico and US Virgin IslandsOfficial notice →US
GlaxoSmithKline LLC recalls Tivicay (dolutegravir) Tablets 50 mg, 30-count Bottle, Rx Only, Manufactured for: ViiV Healthcare RTP, NC 27709, NDC 49702-228-13.
Labeling: incorrect or missing lot and/or expiration date. An incorrect expiration date was printed on the product labeling with an expiration date of January 2027, whereas the correct expiration date is September 2026.
US
Direct Rx recalls Losartan Pot/HCTZ 100/12.5 mg 90 Tabs NDC 72189-290-90 Packaged and Distributed By: Direct Rx Dawsonville, GA 30534 Mfg. For Macleods…
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits .