Acme United Corporation Recalls PhysiciansCare Brand Over-the-Counter Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The recalled over-the-counter products contain regulated substances (aspirin, acetaminophen, or ibuprofen) which must be in child resistant packaging when being used in the household as required by the Poison…
Read the official notice →
- Date
- 2022-03-17
- Country
- United States
- Brand
- Acme United, of Rocky Mount, North Carolina
- Product
- PhysiciansCare brand Aspirin, Extra Strength Non Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station,…
- Units
- About 165,000
- Category
- Drugs & medical
- Source
- CPSC
Copied automatically from the US Consumer Product Safety Commission. Details may be shortened or out of date; the official notice is the authoritative source.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 Consumer Product Safety Commission has the exact models, batch codes and remedy, and it takes priority.
More Acme United, of Rocky Mount, North Carolina recalls
- 2023-05-18
US
Acme United Recalls PhysiciansCare Brand Allergy Relief and Cold and Cough Tablets Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold…
The recalled products contain diphenhydramine hydrochloride and acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not…
Other drugs & medical recalls in the United States
- 2022-03-23
US
B. Braun Medical, Inc. recalls 0.9% Sodium Chloride Injection USP, 250 mL Excel Container, Rx only, B. Braun Medical Inc., Bethlehem, PA, NDC 0264-7800-20
Lack of sterility assurance: leaking bags
US
Golden State Medical Supply Inc. recalls Alprazolam Tablets, USP 1mg, 180-count bottles, Rx only, Manufactured by ULTRAlab Laboratories, Inc., NY; Packaged by GSMS,…
CGMP Deviation: Potential cross-contamination with other drug substance during the manufacturing process.
US
The Harvard Drug Group recalls hydrALAZINE HCl Tablets, USP, 10 mg, 100 Tablets per carton (10x10 blister packs), Rx only, Distributed by: MAJOR PHARMACEUTICALS,…
Failed Impurities/Degradation Specifications: Out of specification result obtained during routine stability testing for Impurities.
- 2022-03-16
US
Ion Beam Applications S.A. recalls ProteusPLUS and ProteusONE- designed to produce and deliver a proton beam for the treatment of patients with localized tumors and…
When resuming from a beam pause, the Proton Therapy System does not verify whether the beam range has not been manually modified during the pause and is still the prescribed one. Therefore, if an operator manually…
FDA · DeviceIon Beam Applications S.A.IL, KS, LA, FL, MI, OK, PA, NJ, TN, TX, VA, WA Foreign: Belgium, England,…Official notice →US
Envisiontec US Llc recalls PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact…
The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product specifications.
US
Physio-Control, Inc. recalls HeartSine Samaritan PAD, SAM 350P Semi-Automatic Defibrillator, used with Pad-Pak
Semi-automatic defibrillators shipped out by Stryker without battery and electrode packs.