3M Company - Health Care Business recalls
39 recalls in our records from 1996 to 2026: 30 FDA medical devices, 8 CPSC, 1 FDA drugs.
Recalls with full detail pages
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3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
The recalled thermal laminators can overheat, posing a fire hazard.
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3M Company Recalls Thermal Laminators Due to Overheating
The recalled thermal laminators may overheat, posing a burn hazard to consumers.
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3M Company medical device recall: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355
Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.
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3M Recalls Peltor X4 Series Earmuffs Due to Risk of Overexposure to Loud Noise and Sound
The recalled noise-reducing earmuffs can develop cracks in the colored portion of the plastic cups, posing a risk of overexposure to loud noise and sound.
Earlier and other recalls
These link to the official agency notice.
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3M Company medical device recall: 3M Ranger Irrigation Fluid Warming Set Official notice ↗
Notice was issued to clarify flow rates related to the inlet fluid temperature.
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3M Company - Health Care Business medical device recall: Clarity Precision Grip Attachments Official notice ↗
Attachments may not mate with the tooth as intended in the digital treatment design.
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3M Company - Health Care Business medical device recall: 3M Tegaderm CHG Official notice ↗
Contamination with foreign substance matter
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3M Company - Health Care Business medical device recall: 3M Durapore Surgical Tape Official notice ↗
Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were incorrectly labeled with a shelf life of 5 years, rather than 3 years.
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3M Company - Health Care Business medical device recall: 3M Tube Securement Device Official notice ↗
Manufacturing nonconformities are in some lots of the Tube Securement Device, such as the top film layer may be partially or completely missing and some devices may…
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3M Company - Health Care Business medical device recall: 3M Specialty Blade Assembly Official notice ↗
3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor…
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3M Company - Health Care Business medical device recall: 3M Attest Super Rapid Readout Biological Indicator Official notice ↗
Specific lots of 3M Attest Super Rapid Readout Biological Indicators (1492V), 3M Attest Super Rapid 5 Steam-Plus Challenge (41482V, 41482VF), and 3M Attest Super Rapid…
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3M Company - Health Care Business medical device recall: 3M Attest Steam Chemical Integrators Official notice ↗
3M Attest Steam Chemical Integrators with dates of manufacture between November 6, 2022 and January 17, 2023 have an increased potential to leak ink during a…
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3M Recalls Scotch™ Thermal Laminators Due to Fire Hazard Official notice ↗
A safety feature can malfunction if the laminator overheats, posing a fire hazard.
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3M Company - Health Care Business medical device recall: 3M Red Dot Electrodes Official notice ↗
Potential for breakage of the ECG electrode carbon stud from the eyelet.
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3M Company - Health Care Business medical device recall: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel -… Official notice ↗
Corrosion could cause performance failures in the product.
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3M Company - Health Care Business medical device recall: 3M Durapore Advanced Official notice ↗
While the product meets all safety and efficacy criteria, long term exposure of 3M Durapore Advanced Surgical Tape to continuous high moisture clinical applications has…
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3M Company - Health Care Business medical device recall: 3M(TM) Surgical Clipper by Remington(R) REF 9602 The 3M Surgical… Official notice ↗
3M has recently received reports involving the 3MTM Surgical Clipper by Remington¿, Model 9602, overheating in mobile/field EMS situations while charging from a modified…
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3M Company - Health Care Business medical device recall: 3M Fast Release Varnish Official notice ↗
Product has an unpleasant flavor due to a manufacturing process error resulting in an extraneous material being introduced into the product.
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Scotch Thermal Laminators Recalled by 3M Due to Burn Hazard Official notice ↗
The plastic enclosure can overheat, posing a burn hazard.
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3M Company - Health Care Business medical device recall: Futuro Official notice ↗
3M discovered that the Futuro" Quick Strap Ankle Brace (Cat. #47736EN) and ACE" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products…
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3M Company - Health Care Business medical device recall: 3M Surgical Clipper Professional 9681 Official notice ↗
Failure to follow proper charging practices can result in lithium-ion battery degradation, characterized by excessive heat during operation or failure to properly…
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3M Company - Health Care Business medical device recall: 3M Bair Hugger(M) Normothermia System Official notice ↗
Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming Blanket, Models 63500 and 63700, can make these blankets more susceptible to unintended occlusion…
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3M Company - Health Care Business medical device recall: Ace(Tm) Brand Official notice ↗
Mold was found on the non-patient contact surfaces of the product and was identified as Aspergillus candidus.
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3M Company - Health Care Business medical device recall: 3M Bair Hugger(TM) Normothermia System Official notice ↗
During a recent investigation, 3M confirmed that a programming translation error could occur in a small amount of the sensors that could lead to a temperature readout…
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3M Company - Health Care Business medical device recall: 3M Ranger(TM) Pressure Infusor Official notice ↗
It was discovered that one Ranger Pressure lnfusor Model 145, SN: 100873, produced a left chamber pressure that was slightly below the manufacturing specification.
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3M Company - Health Care Business medical device recall: 3M Universal Electrosurgical Pad Official notice ↗
3M is recalling Universal Electrosurgical Pads because a report of an unintended material (process liner) in the product. This may prevent or impede the safe return of…
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3M Recalls Hard Hats Due to Shock Hazard Official notice ↗
Hard hats sold online were marketed to protect against electric shock, but they do not provide this protection, posing a shock hazard to consumers.
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3M Company - Health Care Business medical device recall: 3M Steri-Vac Gas Sterilizer/Aerator Official notice ↗
3M discovered a valve with incorrectly labeled "input" and "output" orientation. This defect can result in the valve being installed backwards, creating a remote…
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3M Company - Health Care Business medical device recall: 3M Coban Self-Adherent Wrap Shipper carton label identified the… Official notice ↗
Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to users with sensitivity or allergic reaction…
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3M Company - Health Care Business drug recall: DuraPrep Surgical Solution Iodine Povacrylex Official notice ↗
Chemical contamination: Product may be contaminated with a toxic compound.
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3M Company - Health Care Business medical device recall: Block Versions Used by Dental Offices often referred to as chairside… Official notice ↗
3M is initiating a Field Correction to remove the crown indication from all Lava Ultimate products. These products will continue to be indicated for onlays, inlays and…
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3M Company - Health Care Business medical device recall: 3M Attest Auto-reader. Model numbers 390 Official notice ↗
Labeling on units shipped prior to May 16th, 2014 did not contain the statement "This product contains dry natural rubber" as required by the United States Food and Drug…
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3M Company - Health Care Business medical device recall: 3M" Steri-Vac" Gas Sterilizer/Aerators Official notice ↗
Recently, 3M received a single report of a potential exposure to Ethylene Oxide (EO) at a hospital installation involving 3M" Steri-Vac" Gas Sterilizers. The cause was…
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3M Company - Health Care Business medical device recall: 3M ESPE Imprint II Regular Body Official notice ↗
Specific lots of Imprint II and Paradigm impression material refill packs are being recalled because the moisture displacement feature in both is greatly reduced which…
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3M Company - Health Care Business medical device recall: 3M Espe Official notice ↗
3M is recalling specific lots of 3M ESPE Unitek Primary Stainless Steel Crowns - Series UR4 contain LL3 crowns which are incorrectly labeled as UR4 crowns.
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3M Company - Health Care Business medical device recall: 3M Scotchcast Official notice ↗
3M is conducting a voluntary product recall of selected lots of 3M" Scotchcast" Wet or Dry Cast Padding. Upon investigation of a health care provider feedback, and…
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3M Recalls Filtrete Room Air Purifiers Due to Fire Hazard Official notice ↗
The ion generator in the air purifiers can overheat, posing a fire hazard.
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3M Company - Health Care Business medical device recall: 3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac… Official notice ↗
3M determined that the electrical grounding mechanism for the Steri-Vac 5XL and 8XL gas Sterilizer/Aerator did not meet all of the requirements of the standard in that…
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Overhead Projector Recalled by 3M Official notice ↗
Electrocution/Electric Shock
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.