Smiths Medical ASD Inc. recalls CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L…
Specific Pumps may exhibit intermittent performance in the AILD (Air in Line Detector) function. If an AILD does not sufficiently discern fluid from air in line, an air in line event may not be recognized by the pump…
Read the official notice →- Date
- 2021-10-27
- Country
- United States
- Brand
- Smiths Medical ASD
- Product
- CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c. 21-2120-0105-06L d. 21-2120-0105-07L e.…
- Classification
- Class I
- Units
- Distribution to European countries: BE, BH, CH, DE, DK, ES, FI, FR, GB, IT,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Smiths Medical ASD recalls
- 2021-11-03
US
Smiths Medical ASD Inc. recalls Bivona Aire-Cuf Endotracheal Tube
Inadequate pouch seal leading to a compromised sterile barrier on products with a shaft length of 325mm.
FDA · DeviceSmiths Medical ASD Inc.Worldwide distribution - US Nationwide distribution in the states of AL, AZ,…Official notice →US
Smiths Medical ASD Inc. recalls Pneupac paraPac plus 300 ventilator kit, REF P300NGB
Two devices were labeled with the same serial number
- 2021-10-27
US
Smiths Medical ASD Inc. recalls medfusion Stopcock, 1-way and 4-way, Model Numbers (REF): a. 081-101BE b. 081-101GE c. 081-101GEE d. 081-101NE e. 081-102NE f. 081-102RE…
Product has a lack of sterility assurance
FDA · DeviceSmiths Medical ASD Inc.International Distribution to countries of: Armenia, Austria, Germany, Great…Official notice →US
Smiths Medical ASD Inc. recalls smiths medical portex Loss of Resistance Device, REF 100/398/000
The labeling was missing information on sterilization and prohibition of reuse.
FDA · DeviceSmiths Medical ASD Inc.Canada. Belgium, Great Britain, Ireland, Czech Republic, Spain, France,…Official notice →US
Smiths Medical ASD Inc. recalls CADD Administration Sets, Model #21-7346-24
Product may have been manufactured with an air filter assembled in an incorrect orientation.
- 2021-10-20
US
Smiths Medical ASD Inc. recalls smiths medical medex CBSS-5ML, Triple set, (172/15cm), Model Number DPSHC0092
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
FDA · DeviceSmiths Medical ASD Inc.Austria, France, Germany, Great Britain, and Saudi ArabiaOfficial notice →
Other drugs & medical recalls in the United States
- 2021-10-27
US
Implant Resource Inc recalls MPR Slotted Mallet, labeling etched onto devices as follows: Medical Products Resource 800.524.5194 www.m-p-r.com MPR-1120-1000…
Potential for mallet head to become separated from mallet handle. There is also significant deformations on striking surface that were not expected
US
Fort Defiance Industries, LLC recalls P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641
The rear heater plate and cover assembly that contains the electrical wiring for the heaters does not have sufficient bonding to ground.
FDA · DeviceFort Defiance Industries, LLCDistributed nationwide to PA, MD, TX, NJ, OH, TN, UT, VA and internationally…Official notice →US
Ortho Clinical Diagnostics Inc recalls VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance of the…
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls Outside of Expected Control Range, potential for delayed results
FDA · DeviceOrtho Clinical Diagnostics IncWorldwide Distribution: US (Nationwide) in states of: AL, AR, AZ, CA, CO, DC,…Official notice →US
Datascope Corp. recalls Cardiosave Li-Ion Battery Pack, Part No. 0146-00-0097. Component of the Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) with the below…
A Cardiosave Lithium-Ion Battery Pack used during protocol testing failed to meet the minimum runtime requirement per Getinge internal Product Specification. These nonconforming batteries were inadvertently released to…
FDA · DeviceDatascope Corp.Worldwide distribution. US nationwide, Australia, Brazil, Bahrain, Belgium,…Official notice →US
Lupin Pharmaceuticals Inc. recalls Imipramine Pamoate Capsules 125 mg, 30-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202…
Out of specification result observed in a dissolution test at the 9-month long term stability time point.
US
Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-Release Capsules, 20 mg* (equivalent to 20.6 mg omeprazole magnesium), 24 Hour, 14-count capsules per bottle…
CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.