Wipro GE Healthcare Private Ltd. recalls GE Healthcare neonatal incubator, models: a) Care Plus, b) Care Plus 1000, c) Care Plus 2000, d) Care Plus 3000, e) Care Plus…
GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed…
Read the official notice →- Date
- 2024-02-21
- Country
- United States
- Brand
- Wipro GE Healthcare Private
- Product
- GE Healthcare neonatal incubator, models: a) Care Plus, b) Care Plus 1000, c) Care Plus 2000, d) Care Plus 3000, e) Care Plus 4000, Plus…
- Classification
- Class I
- Units
- Worldwide distribution.
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Wipro GE Healthcare Private recalls
- 2025-10-29
USWipro GE Healthcare Private Ltd. recalls GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical…
Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs…
- 2024-10-02
- US
Wipro GE Healthcare Private Ltd. recalls GE Panda iRES Warmer, Model/Catalog Numbers: 1) M1112198-01045518; 2) M1112198-01045579; 3) M1112198-01047148; 4)…
GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There are multiple electrical safety protections included in the…
FDA · DeviceWipro GE Healthcare Private Ltd.US and Australia, Denmark, France, Germany, Ireland, ITALY, New Zealand,…Official notice →
Other drugs & medical recalls in the United States
- 2024-02-21
- US
Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
FDA · DeviceMusculoskeletal Transplant Foundation, Inc.Product was distributed to Minnesota.Official notice → - US
NeuroLogica Corporation recalls Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.
FDA · DeviceNeuroLogica CorporationUS Nationwide Distribution including states of: AL, AR, CA, CO, CT, DC, FL,…Official notice → - US
Abiomed, Inc. recalls Impella catheters - Intravascular micro axial blood pumps that support a patient's circulatory system. (1) Product Code 005042 - Impella…
IFU has been updated to include warnings about the risk of the inlet perforating through the myocardial wall of the left ventricle due to operator handling.
FDA · DeviceAbiomed, Inc.Worldwide distribution - US Nationwide and the countries of AU, CA, DE, FR,…Official notice → - US
IntegraDose Compounding Services LLC recalls Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx…
Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
- US
The Harvard Drug Group LLC dba Major Pharmaceuticals and… recalls HydrALAZINE Hydrochloride Tablets, USP 10mg, packaged in 100-count (10x10 blister cards), Lot T04680,…
an out of specification result obtained during routine stability testing for Impurities. There is a remote possibility that use of this product could cause a medically reversible or transient adverse health consequences.
FDA · DrugThe Harvard Drug Group LLC dba Major Pharmaceuticals and…The product was distributed nationwide within the United States.Official notice → - US
Teva Pharmaceuticals USA, Inc recalls Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each…
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.