Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 2,226 - 2,250 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 The device does not bear a unique device identifier.	FDA Z-1505-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details
Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antigens in throat swabs. Product not cleared by the FDA.	FDA Z-1561-2026	Medical Device	High	Mar 18, 2026 Recall: Dec 19, 2025	Details
Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable. Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.	FDA Z-1550-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 9, 2026	Details
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1513-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
GEM Premier 5000; Part No. 00055445010 & 00055445011. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1543-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
GEM Premier 5000 PAK; Part No. 00055415004. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1532-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
GEM Premier 5000 PAK; Part No. 00055360010. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1526-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
CLARITY II Laser System; Model No. 1110200210. Reports of devices sparking/popping and potentially burning patients.	FDA Z-1558-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 27, 2026	Details
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT/XALT Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.	FDA Z-1564-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 28, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-2836/11; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1516-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1514-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,L MDTGXP4JXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTGXP4JXXL DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XX MDTL1002862EF DBD-GOWN,SURG,XALT,L4,PANEL CVR,GREEN,XL MDTZ1000893AJ DBD-GOWN,SRG,PNL CVR, GREEN,SNPS,XL Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting may result in brief delay in patient care. If delaminated product is used and surgical strikethrough occurs, there may be risk of infection.	FDA Z-1563-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 28, 2026	Details
GEM Premier 5000; Part No. 00055430011. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1540-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
Endo-Model Replacement Plateau; Item Number: 15-2835/12; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1515-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
IBA Proton Therapy System - PROTEUS 235 It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS does not interrupt the beam delivery if the Healthy Signal from an external gating device is lost. This may lead to a risk of mistreatment when external gating devices are used.	FDA Z-1497-2026	Medical Device	High	Mar 18, 2026 Recall: Feb 3, 2026	Details
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X The device does not bear a unique device identifier.	FDA Z-1499-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details
Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X Impactor handle may be missing cross-pin	FDA Z-1510-2026	Medical Device	High	Mar 18, 2026 Recall: Feb 3, 2026	Details
Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX Kit/RE4001-01, Leader TRUE METRIX Kit/RE4002-01, Leader TRUE METRIX Meter Only/RE4002-40, CVS TRUE METRIX Kit/RE4007-01SB, GNP TRUE METRIX Meter Only/RE4011-00, GNP TRUE METRIX Kit /RE4011-01, MEIJER TRUE METRIX Kit/RE4019-01, FRED'S TRUE METRIX Kit/RE4023-01, DISCOUNT DRUG TRUE METRIX Kit/RE4025-01, KINRAY TRUE METRIX Kit/RE4027-01, HEB TRUE METRIX Kit/RE4031-01, McKesson TRUE METRIX Starter Kit/RE4051-43, SUNMARK TRUE METRIX Meter Only/RE4054-00, The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code description and recommended actions for the E-5 error code in the labeling do not: (a) clearly emphasize that an E-5 error code could represent a very high blood glucose level, and (b) prominently convey the appropriate immediate actions, such as contacting a healthcare professional. This could lead to a delay in treatment if the user does not seek medical attention immediately when receiving an E-5 error code and experiencing symptoms of high glucose.	FDA Z-1545-2026	Medical Device	High	Mar 18, 2026 Recall: Feb 6, 2026	Details
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case. During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.	FDA Z-1496-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 27, 2026	Details
Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci (Strep A) in throat swab samples. Product not cleared by the FDA.	FDA Z-1560-2026	Medical Device	High	Mar 18, 2026 Recall: Dec 19, 2025	Details
Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL The device does not bear a unique device identifier.	FDA Z-1506-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details
GEM Premier 5000; Part No: 00055415011. Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.	FDA Z-1536-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 20, 2026	Details
Penner Pacific Bathing Spa, Model Numbers 860010-1L The device does not bear a unique device identifier.	FDA Z-1508-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details
Endo-Model Replacement Plateau; Item Number: 15-0027/15; The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.	FDA Z-1512-2026	Medical Device	High	Mar 18, 2026 Recall: Jan 12, 2026	Details
Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X The device does not bear a unique device identifier.	FDA Z-1504-2026	Medical Device	High	Mar 18, 2026 Recall: Aug 13, 2025	Details

Showing 2,226 - 2,250 of 3,321 product recalls

Prev 1 ... 88 89 90 91 92 ... 133 Next

Product Recalls Today

Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.

Recent Product Recall Alerts

Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.

High-Risk Recall Updates

High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.

Daily Official Source Coverage

This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.

Latest Recalls By Source Agency

Use the source notes to understand which agency published the notice and what type of product it covers.

CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

How To Use The Latest Product Recalls Page

Check The Publish Date First

Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.

Filter By Product Type

Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.

Prioritize High-Risk Notices

Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.

Verify The Official Notice

Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.

Latest Product Recalls FAQ

Helpful context for searches such as product recalls today, recent product recalls and recall alerts.

How often is the latest product recall list updated?

The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.

Why do some recent recalls have older recall dates?

Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.

What should I check on a recent food recall?

Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.

Can I get only high-risk recalls?

Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.

Find Recent Product Recall Alerts